Multinational Survey of Epidemiology, Morbidity, and Outcomes in Intracerebral Hemorrhage

NCT02567162 | Completed

• 1 other identifier: HSC20150655H
• Study Type: observational
• Target: 40
• Locations: 0 countries
• Sites: N/A

Brief Summary

The aim of this project is development of a comprehensive, prospective, multinational, multicenter, hospital-based, data repository for patients with intracerebral hemorrhage.

Conditions

Intracerebral Hemorrhage

Keywords

Intracerebral hemorrhage; Hemorrhagic stroke; Intraparenchymal hemorrhage; Cerebrovascular disease; Stroke

Outcome Measures

Primary Outcomes (1)

• Modified Rankin Scale score

  90 days

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients hospitalized for ICH will be asked to provide their permission for the use of this information for retrospective research studies directed at ICH; such research to be conducted by the MNEMONICH investigators.

You may qualify if:

• Diagnosis of spontaneous intracerebral hemorrhage (ICH) met by clinical and imaging criteria
• Age 18 and above
• Able to consent

You may not qualify if:

• ICH due to trauma
• ICH due to vascular malformation or aneurysm
• ICH due to brain tumor
• ICH due to underlying infectious lesion (e.g., abscess)

Sponsors & Collaborators

• The University of Texas Health Science Center at San Antonio: lead
• Centre for Cardiovascular Medicine and Cerebrovascular Disease Prevention: collaborator
• Hospital Interzonal de Agudos San Juan Bautista: collaborator
• Maastricht University Medical Center: collaborator
• University of Western Ontario, Canada: collaborator
• Northern Care Alliance NHS Foundation Trust: collaborator
• University of Manchester: collaborator
• University of Rostock: collaborator
• University of Medicine and Pharmacy Craiova: collaborator
• San Camillo de' Lellis General Hospital: collaborator
• Azienda USL Reggio Emilia - IRCCS: collaborator
• University of Central Florida: collaborator
• Manchester Metropolitan University: collaborator

Related Publications (1)

• Behrouz R, Azarpazhooh MR, Godoy DA, Hoffmann MW, Masotti L, Parry-Jones AR, Popa-Wagner A, Schreuder FH, Slevin MA, Smith CJ, Di Napoli M; MNEMONICH Steering Committee. The Multi-National survey on Epidemiology, Morbidity, and Outcomes iN Intracerebral Haemorrhage (MNEMONICH). Int J Stroke. 2015 Dec;10(8):E86. doi: 10.1111/ijs.12629. No abstract available.

  PMID: 26745705 BACKGROUND

MeSH Terms

Conditions

Cerebral Hemorrhage; Hemorrhagic Stroke; Cerebrovascular Disorders; Stroke

Condition Hierarchy (Ancestors)

Intracranial Hemorrhages; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Vascular Diseases; Cardiovascular Diseases; Hemorrhage; Pathologic Processes; Pathological Conditions, Signs and Symptoms

Study Officials

• Mario Di Napoli, MD

  Centre for Cardiovascular Medicine and Cerebrovascular Disease Prevention

  STUDY DIRECTOR

• Mahmoud R Azarpazhooh, MD

  Western University, Canada

  PRINCIPAL INVESTIGATOR

• Reza Behrouz, DO

  The University of Texas Health Science Center at San Antonio

  PRINCIPAL INVESTIGATOR

• Luca Masotti, MD

  Azienda USL Reggio Emilia - IRCCS

  PRINCIPAL INVESTIGATOR

• Adrian R Parry-Jones, MBChB, PhD

  University of Manchester and the Salford Royal NHS Foundation Trust

  PRINCIPAL INVESTIGATOR

• Aurel Popa-Wagner, MD, PhD

  University of Rostock

  PRINCIPAL INVESTIGATOR

• Mark A Slevin, PhD

  Manchester Metropolitan University

  PRINCIPAL INVESTIGATOR

• Craig J Smith, MBChB, MD

  University of Manchester and the Salford Royal NHS Foundation Trust

  PRINCIPAL INVESTIGATOR

• Daniel A Godoy, MD

  Hospital Interzonal de Agudos San Juan Bautista

  PRINCIPAL INVESTIGATOR

• Floris H Schreuder, MD

  Maastricht University Medical Center

  PRINCIPAL INVESTIGATOR

• Michael W Hoffmann, MBChB, PhD

  University of Central Florida

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 90 Days
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Associate Professor

Study Record Dates

• First Submitted: September 30, 2015
• First Posted: October 2, 2015
• Study Start: November 1, 2015
• Primary Completion: August 1, 2016
• Study Completion: August 1, 2016
• Last Updated: December 9, 2016

Record last verified: 2016-12