Evaluation of the Effectiveness of a City Hospital Care Network for the Care of Patients With Transient Ischemic Accident (TIA)
AIT-AMBU-GRE
1 other identifier
observational
51
1 country
1
Brief Summary
Transient ischemic accidents (TIA) are a frequent resort to hospitalization in the emergency department and are serious events in terms of recurrence and handicap. The organization of the "TIA sector" at CHUGA aims to facilitate on the one hand the care of the patient during his hospitalization in the emergencies and on the other hand to allow a safer discharge of the patient as well as his follow-up in ambulatory. The aim of this study is to study the feasibility of comprehensive short-term outpatient management after hospitalization in the emergencies. The research hypothesis is that 90% of patients complete all of the 10 recommended examinations for the diagnosis of TIA, analysis of its risk factors and initiation of necessary treatments, if necessary.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Apr 2022
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 11, 2022
CompletedFirst Posted
Study publicly available on registry
January 31, 2022
CompletedStudy Start
First participant enrolled
April 7, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2022
CompletedMay 24, 2022
January 1, 2022
2 months
January 11, 2022
May 17, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The objective of the research is to study the feasibility of outpatient treatment for TIA from the emergency room, by evaluating the percentage of patients who have completed 100% of the additional examinations included in the course.
The primary endpoint is the mandatory completion of the 10 items recommended by the SFNV and the RENAU, as part of the diagnosis and management of TIA: 1. Recommended standard biology (including assessment of cardiovascular risk factors) 2. The electrocardiogram 3. Brain imaging 4. Imaging of the supraortic trunks 5. The summary of all examinations by a neurologist 6. The introduction of antiplatelet therapy 7. The introduction of statins 8. The follow-up consultation with the attending physician in the month following discharge from the emergency room. 9. Consultation with a cardiologist, with performance of an echocardiography and a Holter ECG 10. Performing a brain MRI
6 months
Secondary Outcomes (4)
Identify the additional examinations that are not performed during the patient's care, and the difficulties in carrying out the standardized care offered to the Emergency Department
6 months
Evaluate the patient's adherence and understanding to the care sector
6 months
Identify the barriers to membership in the care sector
6 months
Identify complications at one month including a recurrence of TIA or stroke
6 months
Study Arms (1)
TIA patients
Diagnostic of TIA by the exams performed in the emergencies of CHUGA.
Interventions
Check of the different exams performed at the emergencies
Eligibility Criteria
Diagnostic of TIA by the exams performed in the emergencies of CHUGA.
You may qualify if:
- Hospitalization in the Emergency Department of the CHUGA for suspicion of TIA
- Possible or probable TIA diagnosis on discharge
- Major patient
- Outpatient care after emergency care
You may not qualify if:
- Protected patient (guardianship, curatorship, people not affiliated with Social Security)
- Patient deprived of liberty by a judicial or administrative decision
- Patient hospitalized without consent under Articles L. 3212-1 and L. 3213-1 which does not fall under the provisions of Article L. 1121-8
- Adult patient subject to a legal protection measure or unable to express consent
- Pregnant, lactating or parturient women
- Patient who does not speak French
- Inability to answer the phone to answer questions
- No attending physician
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU Grenoble Alpes - Urgences
Grenoble, 38100, France
Related Publications (5)
Amarenco P, Benavente O. EXPRESS transient ischemic attack study: speed the process! Stroke. 2008 Aug;39(8):2400-1. doi: 10.1161/STROKEAHA.108.514166. Epub 2008 Jul 3. No abstract available.
PMID: 18599804BACKGROUNDAmarenco P. Not all patients should be admitted to the hospital for observation after a transient ischemic attack. Stroke. 2012 May;43(5):1448-9. doi: 10.1161/STROKEAHA.111.636753. No abstract available.
PMID: 22529312BACKGROUNDAmarenco P, Lavallee PC, Monteiro Tavares L, Labreuche J, Albers GW, Abboud H, Anticoli S, Audebert H, Bornstein NM, Caplan LR, Correia M, Donnan GA, Ferro JM, Gongora-Rivera F, Heide W, Hennerici MG, Kelly PJ, Kral M, Lin HF, Molina C, Park JM, Purroy F, Rothwell PM, Segura T, Skoloudik D, Steg PG, Touboul PJ, Uchiyama S, Vicaut E, Wang Y, Wong LKS; TIAregistry.org Investigators. Five-Year Risk of Stroke after TIA or Minor Ischemic Stroke. N Engl J Med. 2018 Jun 7;378(23):2182-2190. doi: 10.1056/NEJMoa1802712. Epub 2018 May 16.
PMID: 29766771BACKGROUNDLavallee PC, Meseguer E, Abboud H, Cabrejo L, Olivot JM, Simon O, Mazighi M, Nifle C, Niclot P, Lapergue B, Klein IF, Brochet E, Steg PG, Leseche G, Labreuche J, Touboul PJ, Amarenco P. A transient ischaemic attack clinic with round-the-clock access (SOS-TIA): feasibility and effects. Lancet Neurol. 2007 Nov;6(11):953-60. doi: 10.1016/S1474-4422(07)70248-X.
PMID: 17928270BACKGROUNDCucchiara BL, Kasner SE. All patients should be admitted to the hospital after a transient ischemic attack. Stroke. 2012 May;43(5):1446-7. doi: 10.1161/STROKEAHA.111.636746. No abstract available.
PMID: 22529311BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 6 Months
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 11, 2022
First Posted
January 31, 2022
Study Start
April 7, 2022
Primary Completion
June 1, 2022
Study Completion
July 1, 2022
Last Updated
May 24, 2022
Record last verified: 2022-01