Prognosis of a First-Ever Stroke in Persons Living With HIV
NCT ID: NCT02748252
Last Updated: 2018-08-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
TERMINATED
4 participants
OBSERVATIONAL
2015-12-31
2016-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The prognosis of ischemic stroke depends mainly on the care in Stroke Units in the acute phase of the disease (thrombolysis/thrombectomy). It is important that HIV patients are referred to these units in the first hours of a stroke and not to their infectious disease units which is a loss of chance.
It would also be important to know whether HIV patients need specific protocols for stroke emergency management.
The study aims to compare the functional prognosis after the first occurrence of an ischemic stroke, in patients admitted to a Stroke Unit, whether they are infected or not infected by HIV.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Prevalence of Cerebral Small Vessel Disease in HIV Infected Patients
NCT02082574
HIV-1 Infected Adult Subjects With HIV-associated Neurocognitive Disorders Despite Effective Antiretroviral Therapy
NCT04266002
Prevalence, Characteristics and Risk Factors of HIV-Associated Neurocognitive Disorders in Subjects Between the Ages of 55 and 70 Years: An Exposed/Unexposed Cross Sectional Study
NCT02592174
Impact of HIV-infection on Clinical Characteristics and Outcomes on Stroke in Uganda
NCT03072212
HIV&HEART Aging Study (12,5 Year Follow up)
NCT04156048
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
HIV patients
HIV patients admitted in Stroke units for the first occurence of acute stroke
stroke center referral
non HIV patients
non HIV patients admitted in Stroke units for the first occurence of acute stroke
stroke center referral
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
stroke center referral
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* admitted for ischemic stroke, defined as a sudden cerebrovascular event confirmed by MRI
* at least 18 years of age
* paired with patients unexposed to HIV, admitted for ischemic stroke, same gender and age
Exclusion Criteria
* no social security benefits;
* Absence of signed informed consent for the study
* Patients currently pregnant or breast-feeding
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Fondation Ophtalmologique Adolphe de Rothschild
NETWORK
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Fondation Ophtalmologique Adolphe de Rothschild (FOR)
Paris, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AMR_2014-3
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.