Clinical Trials Logo
  1. Home
  2. Informed Consent
  3. NCT05752318
  4. Details
NCT05752318 Clinical Trial

Analysis of the Persistence, Reservoir and HIV Latency

Informed Consent Clinical Trial

— APRIL  

Official title:
APRIL Study: Analysis of the Persistence, Reservoir and HIV Latency

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05752318
Other study ID # 8825
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date February 27, 2023
Est. completion date February 25, 2027

Study information
Verified date January 2023
Source University Hospital, Strasbourg, France
Contact Pierre GANTNER, MCU-PH
Phone 03 69 55 16 32
Email pierre.gantner@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The APRIL study aims at analyzing HIV reservoirs, latency and persistence on antiretroviral therapy. It enrolls HIV-infected adults providing blood samples of which peripheral blood mononuclear cells are stored. The frequency, phenotype and inducibility of HIV-infected cells are then analyzed. These parameters may vary across the different clinical and therapeutic settings.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 500
Est. completion date February 25, 2027
Est. primary completion date January 25, 2027
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - HIV-infection - Adults (>18 years) - Social insurance - Informed consent Exclusion Criteria: - HIV-uninfected - <18 years - Lack of social insurance - Lack or withdraw of consent

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Outcome
Type Measure Description Time frame Safety issue
Primary HIV-Flow 1 day
See also
  Status Clinical Trial Phase
Completed NCT01546194 - A Survey of Patient's Attitudes Towards Consent For Clinical Research In Anesthesiology
Completed NCT00899392 - Improving Informed Consent in Pediatric Endoscopy N/A
Completed NCT05505058 - One-time Informed Consent for Research in Prison N/A
Recruiting NCT06140043 - Augmented Reality for Orthognatic Surgery Patient Education Phase 2/Phase 3
Completed NCT01933139 - Informed Consent for Hysterectomy: Effectiveness of Audio-visual Presentations on Patient Comprehension N/A
Completed NCT00032565 - EQUIC-SM: Enhancing Quality of Informed Consent N/A
Completed NCT01778582 - Perspective-taking, and Examining the Clinical Trial Informed Consent Process
Not yet recruiting NCT06104137 - MOOC Applications Related to Shared Decision Making in Bariatric Surgery N/A
Not yet recruiting NCT04614688 - Assessing the Impact of a Patient Education Platform to Augment the Informed Consent Process for Obstetrics and Gynecology Procedures N/A
Withdrawn NCT02799407 - Electronic Consent of Numerous Subjects Employing Novel Techniques Trial N/A
Completed NCT03960723 - Descriptive Study to Evaluate the Understanding Degree of Informed Consent in Surgical Procedures
Completed NCT03555760 - Patients' Readings of Pre-operative Informed Consent Forms
Completed NCT03405766 - Barriers in the Process of Achieving Informed Consent From Critically Ill Patients
Recruiting NCT06192511 - Implementing a Novel Consent Process for Biospecimen Research After Newborn Screening N/A
Completed NCT02541799 - Comprehension of Research Informed Consent When Applied Through a Telemedicine Medium Phase 2
Completed NCT01635842 - Informed Consent and Clinical Trials N/A
Withdrawn NCT02332837 - Interactive Tool for Informed Consent N/A
Completed NCT02885532 - Capacity to Consent in Acutely Intoxicated Emergency Department Patients N/A
Completed NCT04627597 - Patients' Comprehension and Internalization of Operative Consent Form
Completed NCT03503487 - Surgical Planning and Informed Consent N/A