CENTER-TBI: Collaborative European NeuroTrauma Effectiveness Research in TBI
CENTER-TBI
Collaborative European NeuroTrauma Effectiveness Research in TBI (CENTER-TBI)
1 other identifier
observational
4,559
18 countries
63
Brief Summary
The research aims of the CENTER-TBI study are to:
- 1.better characterize Traumatic Brain Injury (TBI) as a disease and describe it in a European context, and
- 2.identify the most effective clinical interventions for managing TBI.
- 3.To collect high quality clinical and epidemiological data with repositories for neuro-imaging, DNA, and serum from patients with TBI.
- 4.To refine and improve outcome assessment and develop health utility indices for TBI.
- 5.To develop multidimensional approaches to characterisation and prediction of TBI.
- 6.To define patient profiles which predict efficacy of specific interventions ("Precision Medicine").
- 7.To develop performance indicators for quality assurance and quality improvement in TBI care.
- 8.To validate the common data elements (CDEs) for broader use in international settings, and to develop a user-friendly web based data entry instrument and case report form builder.
- 9.To develop an open database compatible with Federal Interagency Traumatic Brain Injury Research (FITBIR).
- 10.To intensify networking activities and international collaborations in TBI.
- 11.To disseminate study results and management recommendations for TBI to health care professionals, policy makers and consumers, aiming to improve health care for TBI at individual and population levels.
- 12.To develop a "knowledge commons" for TBI, integrating CENTER-TBI outputs into systematic reviews.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2014
Longer than P75 for all trials
63 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 29, 2014
CompletedFirst Posted
Study publicly available on registry
August 6, 2014
CompletedStudy Start
First participant enrolled
December 19, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2018
CompletedResults Posted
Study results publicly available
September 25, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2021
CompletedNovember 7, 2022
April 1, 2022
3.7 years
July 29, 2014
April 6, 2020
April 6, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Glasgow Outcome Scale - Extended (GOSE) at 6 Months
The Extended Glasgow Outcome Scale is a global scale for functional outcome that rates patient status into 8 categories, going from dead to good recovery. 1. Death 2. Vegetative sate 3. Lower severe disability 4. Upper severe disability 5. Lower moderate disability 6. Upper moderate disability - some disability but can potentially return to some form of employment 7. Lower good recovery - minor physical or mental defect 8. Upper good recovery - full recovery The 6-month GOSE score is available in 3804 patients (84%).
6 months
SF-12v2 Health Survey (Short-Form Health Survey With 12 Questions) at 6 Months
The SF-12v2 Health Survey uses 12 questions to measure functional health and well-being from the patient's point of view. The SF-12v2 at 6 months is available in 2300 patients.
6 months
6 Month Quality of Life in Brain Injury (Qolibri-OS) <52 (Impaired)
The Quality of Life in Brain Injury (Qolibri-OS) is a 6 item overall scale that provides a profile of health-related quality of life in domains typicality affected by brain injury, such as physical function, cognition, emotional status, ability to perform daily activities, personal life and social relationship, and satisfaction with current situation and future prospects. The QOLIBRI scores are reported on a 0-100 scale , where 0=worst possible quality of life and 100=best possible quality of life.
6 months
Secondary Outcomes (15)
6 Month Post-traumatic Stress Disorder (PTSD) Checklist for DSM-5 (PCL-5) <33 (Impaired)
6 months
6 Month Rivermead Post Concussion Questionnaire <16 (Impaired)
6 months
6 Month Galveston Orientation and Amnesia Test (GOAT) < 75 (Impaired)
6 months
6 Month Rey Auditory Verbal Learning Test (RAVLT) - Impaired
6 months
6 Month Timed up and go Test - Impaired
6 months
- +10 more secondary outcomes
Eligibility Criteria
Patients presenting with traumatic brain injury. The data collection will be stratified upon enrolment into 3 clinical groups differentiated by clinical care path: * ER stratum: patients seen and discharged from the ER * Admission stratum: patients admitted to hospital but not to the ICU * ICU stratum: patients admitted directly to the ICU
You may qualify if:
- Clinical diagnosis of TBI
- Clinical indication for CT scan
- Presentation within 24 hours of injury
- Informed consent obtained according to local and national requirements
You may not qualify if:
- Severe pre-existing neurological disorder that would confound outcome assessments
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Hospital, Antwerplead
- University of Cambridgecollaborator
- Erasmus Medical Centercollaborator
- San Gerardo Hospitalcollaborator
- University of Sheffieldcollaborator
- University of California, San Franciscocollaborator
- Karolinska Institutetcollaborator
- ICON plccollaborator
- GABO:micollaborator
- icometrixcollaborator
Study Sites (65)
Innsbruck Medical University
Innsbruck, Austria
Medical University Vienna
Vienna, Austria
Antwerp University Hospital
Edegem, Belgium
University Hospitals Leuven
Leuven, Belgium
CHR Citadelle
Liège, Belgium
CHU Liege
Liège, Belgium
Region Hovedstaden Rigshospitalet
Copenhagen, Denmark
Odense University Hospital
Odense, Denmark
Helsinki University Central Hospital
Helsinki, Finland
Turku University Hospital
Turku, Finland
University Hospital of Grenoble
Grenoble, France
Lille University Hospital
Lille, France
University Hospital Nancy
Nancy, France
APHP
Paris, France
CHU Poitiers
Poitiers, France
University Hospital Aachen
Aachen, Germany
Charité Campus Virchow
Berlin, Germany
University Hospital Heidelberg
Heidelberg, Germany
Klinikum Ludwigsburg
Ludwigsburg, Germany
University of Pecs
Pécs, Hungary
University of Szeged
Szeged, Hungary
Rambam Medical Center
Haifa, Israel
Hadassah-hebrew University Medical Center
Jerusalem, Israel
Bufalini Hospital
Cesena, Italy
Fondazione IRCCS CĂ Granda Ospedale Maggiore Poloclinico
Milan, Italy
Niguarda Hospital
Milan, Italy
S Raffaele University Hospital
Milan, Italy
ASST di Monza
Monza, Italy
Maggiore Della CaritĂ Hospital
Novara, Italy
Azienda Ospedaliera UniversitĂ di Padova
Padua, Italy
AOU CittĂ della Salute e della Scienza di Torino
Torino, Italy
Rezekne Hospital
Rēzekne, Latvia
Pauls Stradins Clinical University Hospital
Riga, Latvia
Riga Eastern Clinical University Hospital
Riga, Latvia
University of Health Sciences
Kaunas, Lithuania
Center of neurovascular surgery, Clinic of neurology and neurosurgery, Vilnius University
Vilnius, Lithuania
Kaunas University of technology and Vilnius University
Vilnius, Lithuania
University Medical Center Groningen
Groningen, Netherlands
Leiden University Medical Center
Leiden, Netherlands
Radboud University Medical Center
Nijmegen, Netherlands
Erasmus MC
Rotterdam, Netherlands
Medical Center Haaglanden
The Hague, Netherlands
The HAGA Hospital
The Hague, Netherlands
TweeSteden Ziekenhuis
Tilburg, Netherlands
Oslo University Hospital
Oslo, Norway
University Hospital Northern Norway
Tromsø, Norway
St Olavs Hospital/Norwegian University of science and technology
Trondheim, Norway
Emergency County Hospital Timisoara
Timișoara, Romania
Clinical centre of Vojvodina
Novi Sad, Serbia
Vall d'Hebron University Hospital
Barcelona, Spain
Cruces University Hospital
Bilbao, Spain
Hospital Universitario 12 de Octubre
Madrid, Spain
ClĂnico Universitario de Valencia
Valencia, Spain
Karolinska University Hospital
Stockholm, Sweden
Umea University Hospital
UmeĂ¥, Sweden
Centre Hospitalier Universitaire Vaudois
Lausanne, Switzerland
Queen Elizabeth Hospital
Birmingham, United Kingdom
Southmead Hospital
Bristol, United Kingdom
Addenbrookes Hospital
Cambridge, United Kingdom
Lothian Health Board
Edinburgh, United Kingdom
The Walton centre NHS Foundation Trust
Liverpool, United Kingdom
Kings college London
London, United Kingdom
Salford Royal Hospital
Salford, United Kingdom
Sheffield Teaching Hospitals NHS Foundation Trust
Sheffield, United Kingdom
University Hospitals Southampton NHS Trust
Southampton, United Kingdom
Related Publications (32)
Jacob L, Castro J, Heslot C, Andelic N, Tenovuo O; CENTER-TBI Participants and Investigators (Appendix); Azouvi P. Absence from work in the 12 months following mild traumatic brain injury in Europe: a CENTER-TBI cohort study. Ann Phys Rehabil Med. 2025 Nov;68(8):102017. doi: 10.1016/j.rehab.2025.102017. Epub 2025 Sep 30.
PMID: 41032948DERIVEDKals M, Wilson L, Levey DF, Parodi L, Steyerberg EW, Richardson S, He F, Sun X, Jain S, Palotie A, Ripatti S, Rosand J, Manley GT, Maas AIR, Stein MB, Menon DK; Genetic Associations In Neurotrauma (GAIN) Consortium (with contribution from the CENTER-TBI and TRACK-TBI studies). Genetic vulnerability and adverse mental health outcomes following mild traumatic brain injury: a meta-analysis of CENTER-TBI and TRACK-TBI cohorts. EClinicalMedicine. 2024 Dec 5;78:102956. doi: 10.1016/j.eclinm.2024.102956. eCollection 2024 Dec.
PMID: 39720422DERIVEDGuglielmi A, Graziano F, Bogossian EG, Turgeon AF, Taccone FS, Citerio G; CENTER-TBI Participants and Investigators. Haemoglobin values, transfusion practices, and long-term outcomes in critically ill patients with traumatic brain injury: a secondary analysis of CENTER-TBI. Crit Care. 2024 Jun 14;28(1):199. doi: 10.1186/s13054-024-04980-6.
PMID: 38877571DERIVEDPisica D, Volovici V, Yue JK, van Essen TA, den Boogert HF, Vande Vyvere T, Haitsma I, Nieboer D, Markowitz AJ, Yuh EL, Steyerberg EW, Peul WC, Dirven CMF, Menon DK, Manley GT, Maas AIR, Lingsma HF; CENTER-TBI Participants and Investigators. Clinical and Imaging Characteristics, Care Pathways, and Outcomes of Traumatic Epidural Hematomas: A Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury Study. Neurosurgery. 2024 Nov 1;95(5):986-999. doi: 10.1227/neu.0000000000002982. Epub 2024 May 21.
PMID: 38771081DERIVEDVreeburg RJG, Singh RD, van Erp IAM, Korhonen TK, Yue JK, Mee H, Timofeev I, Kolias A, Helmy A, Depreitere B, Moojen WA, Younsi A, Hutchinson P, Manley GT, Steyerberg EW, de Ruiter GCW, Maas AIR, Peul WC, van Dijck JTJM, den Boogert HF, Posti JP, van Essen TA; for the CENTER-TBI Participants and Investigators. Early versus delayed cranioplasty after decompressive craniectomy in traumatic brain injury: a multicenter observational study within CENTER-TBI and Net-QuRe. J Neurosurg. 2024 Apr 26;141(4):895-907. doi: 10.3171/2024.1.JNS232172. Print 2024 Oct 1.
PMID: 38669706DERIVEDHowe EI, Andelic N, Brunborg C, Zeldovich M, Helseth E, Skandsen T, Olsen A, Fure SCR, Theadom A, Rauen K, Madsen BA, Jacobs B, van der Naalt J, Tartaglia MC, Einarsen CE, Storvig G, Tronvik E, Tverdal C, von Steinbuchel N, Roe C, Hellstrom T; CENTER-TBI Participants and Investigators. Frequency and predictors of headache in the first 12 months after traumatic brain injury: results from CENTER-TBI. J Headache Pain. 2024 Mar 25;25(1):44. doi: 10.1186/s10194-024-01751-0.
PMID: 38528477DERIVEDZeldovich M, Bockhop F, Covic A, Mueller I, Polinder S, Mikolic A, van der Vlegel M, von Steinbuechel N; CENTER-TBI participants and investigators. Factorial validity and comparability of the six translations of the Rivermead Post-Concussion Symptoms Questionnaire translations: results from the CENTER-TBI study. J Patient Rep Outcomes. 2023 Sep 8;7(1):90. doi: 10.1186/s41687-023-00632-5.
PMID: 37682406DERIVEDvan Essen TA, van Erp IAM, Lingsma HF, Pisica D, Yue JK, Singh RD, van Dijck JTJM, Volovici V, Younsi A, Kolias A, Peppel LD, Heijenbrok-Kal M, Ribbers GM, Menon DK, Hutchinson PJA, Manley GT, Depreitere B, Steyerberg EW, Maas AIR, de Ruiter GCW, Peul WC; CENTER-TBI Investigators and Participants. Comparative effectiveness of decompressive craniectomy versus craniotomy for traumatic acute subdural hematoma (CENTER-TBI): an observational cohort study. EClinicalMedicine. 2023 Aug 9;63:102161. doi: 10.1016/j.eclinm.2023.102161. eCollection 2023 Sep.
PMID: 37600483DERIVEDLang L, Wang T, Xie L, Yang C, Skudder-Hill L, Jiang J, Gao G, Feng J. An independently validated nomogram for individualised estimation of short-term mortality risk among patients with severe traumatic brain injury: a modelling analysis of the CENTER-TBI China Registry Study. EClinicalMedicine. 2023 Apr 28;59:101975. doi: 10.1016/j.eclinm.2023.101975. eCollection 2023 May.
PMID: 37180469DERIVEDHowe EI, Zeldovich M, Andelic N, von Steinbuechel N, Fure SCR, Borgen IMH, Forslund MV, Hellstrom T, Soberg HL, Sveen U, Rasmussen M, Kleffelgaard I, Tverdal C, Helseth E, Lovstad M, Lu J, Arango-Lasprilla JC, Tenovuo O, Azouvi P, Dawes H, Roe C; CENTER-TBI participants and investigators. Rehabilitation and outcomes after complicated vs uncomplicated mild TBI: results from the CENTER-TBI study. BMC Health Serv Res. 2022 Dec 16;22(1):1536. doi: 10.1186/s12913-022-08908-0.
PMID: 36527074DERIVEDRezoagli E, Petrosino M, Rebora P, Menon DK, Mondello S, Cooper DJ, Maas AIR, Wiegers EJA, Galimberti S, Citerio G; CENTER-TBI, OzENTER-TBI Participants and Investigators. High arterial oxygen levels and supplemental oxygen administration in traumatic brain injury: insights from CENTER-TBI and OzENTER-TBI. Intensive Care Med. 2022 Dec;48(12):1709-1725. doi: 10.1007/s00134-022-06884-x. Epub 2022 Oct 20.
PMID: 36264365DERIVEDAkerlund CAI, Holst A, Stocchetti N, Steyerberg EW, Menon DK, Ercole A, Nelson DW; CENTER-TBI Participants and Investigators. Clustering identifies endotypes of traumatic brain injury in an intensive care cohort: a CENTER-TBI study. Crit Care. 2022 Jul 27;26(1):228. doi: 10.1186/s13054-022-04079-w.
PMID: 35897070DERIVEDVolovici V, Pisica D, Gravesteijn BY, Dirven CMF, Steyerberg EW, Ercole A, Stocchetti N, Nelson D, Menon DK, Citerio G, van der Jagt M, Maas AIR, Haitsma IK, Lingsma HF; CENTER-TBI investigators, participants for the ICU stratum. Comparative effectiveness of intracranial hypertension management guided by ventricular versus intraparenchymal pressure monitoring: a CENTER-TBI study. Acta Neurochir (Wien). 2022 Jul;164(7):1693-1705. doi: 10.1007/s00701-022-05257-z. Epub 2022 Jun 1.
PMID: 35648213DERIVEDvan Essen TA, Lingsma HF, Pisica D, Singh RD, Volovici V, den Boogert HF, Younsi A, Peppel LD, Heijenbrok-Kal MH, Ribbers GM, Walchenbach R, Menon DK, Hutchinson P, Depreitere B, Steyerberg EW, Maas AIR, de Ruiter GCW, Peul WC; CENTER-TBI Collaboration Group. Surgery versus conservative treatment for traumatic acute subdural haematoma: a prospective, multicentre, observational, comparative effectiveness study. Lancet Neurol. 2022 Jul;21(7):620-631. doi: 10.1016/S1474-4422(22)00166-1. Epub 2022 May 5.
PMID: 35526554DERIVEDHolthe IL, Dahl HM, Rohrer-Baumgartner N, Eichler S, Elseth MF, Holthe O, Berntsen T, Yeates KO, Andelic N, Lovstad M. Neuropsychological Impairment, Brain Injury Symptoms, and Health-Related Quality of Life After Pediatric TBI in Oslo. Front Neurol. 2022 Jan 28;12:719915. doi: 10.3389/fneur.2021.719915. eCollection 2021.
PMID: 35153967DERIVEDHuijben JA, Pisica D, Ceyisakar I, Stocchetti N, Citerio G, Maas AIR, Steyerberg EW, Menon DK, van der Jagt M, Lingsma HF. Pharmaceutical Venous Thrombosis Prophylaxis in Critically Ill Traumatic Brain Injury Patients. Neurotrauma Rep. 2022 Jan 7;2(1):4-14. doi: 10.1089/neur.2021.0037. eCollection 2022.
PMID: 35112104DERIVEDGalimberti S, Graziano F, Maas AIR, Isernia G, Lecky F, Jain S, Sun X, Gardner RC, Taylor SR, Markowitz AJ, Manley GT, Valsecchi MG, Bellelli G, Citerio G; CENTER-TBI and TRACK-TBI participants and investigators. Effect of frailty on 6-month outcome after traumatic brain injury: a multicentre cohort study with external validation. Lancet Neurol. 2022 Feb;21(2):153-162. doi: 10.1016/S1474-4422(21)00374-4.
PMID: 35065038DERIVEDPuybasset L, Perlbarg V, Unrug J, Cassereau D, Galanaud D, Torkomian G, Battisti V, Lefort M, Velly L, Degos V, Citerio G, Bayen E, Pelegrini-Issac M; MRI-COMA Investigators CENTER-TBI MRI Participants and MRI Only Investigators. Prognostic value of global deep white matter DTI metrics for 1-year outcome prediction in ICU traumatic brain injury patients: an MRI-COMA and CENTER-TBI combined study. Intensive Care Med. 2022 Feb;48(2):201-212. doi: 10.1007/s00134-021-06583-z. Epub 2022 Dec 14.
PMID: 34904191DERIVEDCiterio G, Robba C, Rebora P, Petrosino M, Rossi E, Malgeri L, Stocchetti N, Galimberti S, Menon DK; Center-TBI participants and investigators. Management of arterial partial pressure of carbon dioxide in the first week after traumatic brain injury: results from the CENTER-TBI study. Intensive Care Med. 2021 Sep;47(9):961-973. doi: 10.1007/s00134-021-06470-7. Epub 2021 Jul 24.
PMID: 34302517DERIVEDRobba C, Rebora P, Meyfroidt G, Citerio G. The authors reply. Crit Care Med. 2021 May 1;49(5):e554-e555. doi: 10.1097/CCM.0000000000004961. No abstract available.
PMID: 33854024DERIVEDHuijben JA, Dixit A, Stocchetti N, Maas AIR, Lingsma HF, van der Jagt M, Nelson D, Citerio G, Wilson L, Menon DK, Ercole A; CENTER-TBI investigators and participants. Use and impact of high intensity treatments in patients with traumatic brain injury across Europe: a CENTER-TBI analysis. Crit Care. 2021 Feb 23;25(1):78. doi: 10.1186/s13054-020-03370-y.
PMID: 33622371DERIVEDBorgen IMH, Roe C, Brunborg C, Tenovuo O, Azouvi P, Dawes H, Majdan M, Ranta J, Rusnak M, Wiegers EJA, Tverdal C, Jacob L, Cogne M, von Steinbuechel N, Andelic N; CENTER-TBI participants investigators. Care transitions in the first 6months following traumatic brain injury: Lessons from the CENTER-TBI study. Ann Phys Rehabil Med. 2021 Nov;64(6):101458. doi: 10.1016/j.rehab.2020.10.009. Epub 2021 Jul 23.
PMID: 33246186DERIVEDRobba C, Banzato E, Rebora P, Iaquaniello C, Huang CY, Wiegers EJA, Meyfroidt G, Citerio G; Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury (CENTER-TBI) ICU Participants and Investigators. Acute Kidney Injury in Traumatic Brain Injury Patients: Results From the Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury Study. Crit Care Med. 2021 Jan 1;49(1):112-126. doi: 10.1097/CCM.0000000000004673.
PMID: 33060506DERIVEDGravesteijn BY, Sewalt CA, Nieboer D, Menon DK, Maas A, Lecky F, Klimek M, Lingsma HF; CENTER-TBI collaborators. Tracheal intubation in traumatic brain injury: a multicentre prospective observational study. Br J Anaesth. 2020 Oct;125(4):505-517. doi: 10.1016/j.bja.2020.05.067. Epub 2020 Jul 31.
PMID: 32747075DERIVEDGao G, Wu X, Feng J, Hui J, Mao Q, Lecky F, Lingsma H, Maas AIR, Jiang J; China CENTER-TBI Registry Participants. Clinical characteristics and outcomes in patients with traumatic brain injury in China: a prospective, multicentre, longitudinal, observational study. Lancet Neurol. 2020 Aug;19(8):670-677. doi: 10.1016/S1474-4422(20)30182-4.
PMID: 32702336DERIVEDRobba C, Rebora P, Banzato E, Wiegers EJA, Stocchetti N, Menon DK, Citerio G; Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury Participants and Investigators. Incidence, Risk Factors, and Effects on Outcome of Ventilator-Associated Pneumonia in Patients With Traumatic Brain Injury: Analysis of a Large, Multicenter, Prospective, Observational Longitudinal Study. Chest. 2020 Dec;158(6):2292-2303. doi: 10.1016/j.chest.2020.06.064. Epub 2020 Jul 4.
PMID: 32634435DERIVEDRiemann L, Beqiri E, Smielewski P, Czosnyka M, Stocchetti N, Sakowitz O, Zweckberger K, Unterberg A, Younsi A; CENTER-TBI High Resolution ICU (HR ICU) Sub-Study Participants and Investigators. Low-resolution pressure reactivity index and its derived optimal cerebral perfusion pressure in adult traumatic brain injury: a CENTER-TBI study. Crit Care. 2020 May 26;24(1):266. doi: 10.1186/s13054-020-02974-8.
PMID: 32456684DERIVEDGravesteijn BY, Nieboer D, Ercole A, Lingsma HF, Nelson D, van Calster B, Steyerberg EW; CENTER-TBI collaborators. Machine learning algorithms performed no better than regression models for prognostication in traumatic brain injury. J Clin Epidemiol. 2020 Jun;122:95-107. doi: 10.1016/j.jclinepi.2020.03.005. Epub 2020 Mar 20.
PMID: 32201256DERIVEDHuijben JA, Wiegers EJA, Ercole A, de Keizer NF, Maas AIR, Steyerberg EW, Citerio G, Wilson L, Polinder S, Nieboer D, Menon D, Lingsma HF, van der Jagt M; CENTER-TBI investigators and participants for the ICU stratum. Quality indicators for patients with traumatic brain injury in European intensive care units: a CENTER-TBI study. Crit Care. 2020 Mar 4;24(1):78. doi: 10.1186/s13054-020-2791-0.
PMID: 32131882DERIVEDVan Essen TA, Volovici V, Cnossen MC, Kolias A, Ceyisakar I, Nieboer D, Peppel LD, Heijenbrok-Kal M, Ribbers G, Menon D, Hutchinson P, Depreitere B, de Ruiter GCW, Lingsma HF, Steyerberg EW, Maas AI, Peul WC. Comparative effectiveness of surgery in traumatic acute subdural and intracerebral haematoma: study protocol for a prospective observational study within CENTER-TBI and Net-QuRe. BMJ Open. 2019 Oct 16;9(10):e033513. doi: 10.1136/bmjopen-2019-033513.
PMID: 31619435DERIVEDSteyerberg EW, Wiegers E, Sewalt C, Buki A, Citerio G, De Keyser V, Ercole A, Kunzmann K, Lanyon L, Lecky F, Lingsma H, Manley G, Nelson D, Peul W, Stocchetti N, von Steinbuchel N, Vande Vyvere T, Verheyden J, Wilson L, Maas AIR, Menon DK; CENTER-TBI Participants and Investigators. Case-mix, care pathways, and outcomes in patients with traumatic brain injury in CENTER-TBI: a European prospective, multicentre, longitudinal, cohort study. Lancet Neurol. 2019 Oct;18(10):923-934. doi: 10.1016/S1474-4422(19)30232-7.
PMID: 31526754DERIVEDMaas AI, Menon DK, Steyerberg EW, Citerio G, Lecky F, Manley GT, Hill S, Legrand V, Sorgner A; CENTER-TBI Participants and Investigators. Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury (CENTER-TBI): a prospective longitudinal observational study. Neurosurgery. 2015 Jan;76(1):67-80. doi: 10.1227/NEU.0000000000000575.
PMID: 25525693DERIVED
Related Links
Biospecimen
whole blood samples
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Prof. Em. Dr Andrew Maas
- Organization
- UZA
Study Officials
- STUDY CHAIR
Andrew Maas, MD, PhD
Antwerp University Hospital / University of Antwerp, Edegem, Belgium
- STUDY DIRECTOR
David Menon, MD, PhD
University of Cambridge, Addenbrookes hospital, Cambridge, UK
Publication Agreements
- PI is Sponsor Employee
- No
- Restriction Type
- LTE60
- Restrictive Agreement
- Yes
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 6 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- M.D., PhD, Project Coordinator CENTER-TBI
Study Record Dates
First Submitted
July 29, 2014
First Posted
August 6, 2014
Study Start
December 19, 2014
Primary Completion
September 1, 2018
Study Completion
March 31, 2021
Last Updated
November 7, 2022
Results First Posted
September 25, 2020
Record last verified: 2022-04
Data Sharing
- IPD Sharing
- Will share