Skip to main content
Clinical Trials/NCT02748252
NCT02748252TerminatedNot Applicable

Prognosis of a First-Ever Stroke in Persons Living With HIV

Fondation Ophtalmologique Adolphe de Rothschild1 site in 1 country4 target enrollmentStarted: December 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
4
Locations
1
Primary Endpoint
degree of disability measured with the modified Rankin Scale

Study Overview

Brief Summary

With aging of the persons living with HIV, cardiovascular diseases now account for substantial mortality and morbidity. Stroke frequency grows exponentially with aging and its incidence doubles every decade over 55 years of age.

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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients unexposed to HIV: HIV-1 seronegative OR patients exposed to HIV: HIV seropositive for over 6 months with or without antiretroviral treatment. Confirmed by Elisa and Western blot tests
  • 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

  • antecedents of a symptomatic ischemic or hemorrhagic cerebrovascular event
  • no social security benefits;
  • Absence of signed informed consent for the study
  • Patients currently pregnant or breast-feeding

Outcomes

Primary Outcomes

degree of disability measured with the modified Rankin Scale

Time Frame: 3 months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Network
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials

Prognosis of a First-Ever Stroke in... | Clinical Trial