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Cohort of Young Adults Infected With HIV Since Birth or During Childhood (CO19 COVERTE)

Primary Purpose

HIV Infection, Young Adult

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
blood sampling, specific biological exams and biobank and self administered questionnaires
Sponsored by
French National Agency for Research on AIDS and Viral Hepatitis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for HIV Infection focused on measuring teenagers to adult transition, comparison

Eligibility Criteria

18 Years - 25 Years (Adult)All SexesAccepts Healthy Volunteers

Group of HIV Infection

Inclusion Criteria:

  • Age ≥ 18 and < 25 years
  • Able to give written consent
  • Covered by French Social Security
  • diagnosis of HIV-1 et/ou-2 documented before age 13

Exclusion Criteria (for physiopathological module only)

  • Under protection(saving) of justice

Control Group

Inclusion Criteria:

  • Age ≥ 18 and ≤ 25 years
  • Able to give written consent
  • Covered by French Social Security
  • With a brother or sister, cousin, father or mother HIV infected, inbred or adopted
  • With a negative serology for HIV infection, HBV, HCV
  • Without diabetes mellitus
  • able to go to Clinical Investigation Center of Necker and to Hospital St. Antoine for the recruitment and monitoring

Exclusion Criteria:

  • Under protection(saving) of justice

Sites / Locations

  • Hôpitaux (voir liste jointe)

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

HIV infected

HIV uninfected

Arm Description

young adult infected by HIV

a control group of HIV uninfected young adult will be included for comparison in physiopathological module (metabolic, cardiovascular, and immunological)

Outcomes

Primary Outcome Measures

Immuno virological and clinical prognosis: HIV RNA <50c/mL, CD4 cells count>500 cells/mL, vital status, CDC stage

Secondary Outcome Measures

Professional and schooling integration, social life:marital status, type of accommodation, education level, type and age at first employment
sexuality, sexual risk behaviour: age at first intercourse, condom use at first, last sexual intercourse, and during last year, unplanned pregnancy, interruption of pregnancy
metabolic and cardiovascular abnormalities: abnormalities in glucose tolerance and insulino-resistance, dyslipidemia, lipodystrophy, adipocyte dysfunction, atherosclerosis,dysfunction, median of intima media thickness and pulse wave velocity
Lymphocyte phenotype and functional capacity of T lymphocyte: description of dysfunctional CMV-specific T cell, T cell responses measured at inclusion, and their evolution during follow-up

Full Information

First Posted
September 17, 2010
Last Updated
December 4, 2020
Sponsor
French National Agency for Research on AIDS and Viral Hepatitis
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1. Study Identification

Unique Protocol Identification Number
NCT01269632
Brief Title
Cohort of Young Adults Infected With HIV Since Birth or During Childhood
Acronym
CO19 COVERTE
Official Title
Long Term Evaluation of Young Adults Born to HIV-infected Mothers. A Cohort of Young Adults Infected With HIV Since Birth or During Childhood
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
June 2010 (undefined)
Primary Completion Date
December 2018 (Actual)
Study Completion Date
December 27, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
French National Agency for Research on AIDS and Viral Hepatitis

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: With the improvement of the prognosis for HIV-infected infants, thanks to the availability of antiretroviral therapies, young adults infected with HIV since birth are becoming an emerging group among the HIV-infected population. Morbidity, mortality and immunovirological evolution in these young adults need to be studied in a large population and compared to patients infected with HIV later in adulthood or to the general population in terms of mortality. Moreover, the study of accelerated or premature ageing, linked to HIV and/or antiretroviral therapy, is particularly interesting in this population. Objectives: To study the transition to adulthood and the further evolution of HIV-1 or -2 perinatally infected young adults: 1) To study the teenager to adult transition in terms of clinical and immunovirological status, schooling and professional integration, sexuality and reproductive life, transition from paediatrics to adult departments; 2) To study prognosis, morbidity and mortality according to age, infection stage at the time of antiretroviral initiation and therapeutic history; 3) To study the incidence and expression of adverse events and the potential link to antiretroviral therapies; 4) To study the markers of a potential premature ageing, from the metabolic, cardiovascular and immunological points of view.
Detailed Description
Methods: A national multicenter cohort of young adults, infected with HIV since birth or during childhood, including a common module and a physiopathological module (metabolic,, cardiovascular and immunological). A control group of HIV-uninfected young adults is included for comparison in the latter module. Patients aged between 18 and 25 years of age, whose HIV diagnosis was made before the age of 13 are eligible for ANRS CO19 COVERTE. This cohort is an extension of the EPF cohort (ANRS CO10), in which follow-up stops at the age 18, with an extension to adults with a HIV diagnosis established before the age of 13. Questionnaires are filled out by physicians once a year. Self-administered questionnaires are also carried out. Blood sampling and specific biological exams are collected and a biobank constituted. In the physiopathological module, specific exams are carried out at inclusion and after 3 years of follow-up: metabolic and immunological exams, OGTT, CT-scan and DXA-scan, and cardiovascular explorations (carotid intima-media thickness, pulse wave velocity …). An estimated 400 enrolments during the first 3 years is expected in the common module and an estimated 200 HIV-infected subjects and 75 uninfected controls is expected in the physiopathological module. Expected results: The follow-up of young adults in this cohort will bring new data on the long term efficacy of antiretroviral treatment and their adverse events, from the metabolic, cardiovascular and immunological, point of view, be they linked or not to HIV infection per se. This analysis will take into account the characteristics of this population, as compared to adults infected during adulthood: an early exposure to HIV and antiretroviral treatment, a different social context, difficulties in care, and a different exposure to risk factors for adverse events and complications. We will evaluate the impact of the transition to adulthood and of the transition from paediatrics to adult departments, on clinical prognosis, adherence, professional and schooling integration, sexuality, social life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infection, Young Adult
Keywords
teenagers to adult transition, comparison

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
469 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HIV infected
Arm Type
Other
Arm Description
young adult infected by HIV
Arm Title
HIV uninfected
Arm Type
Other
Arm Description
a control group of HIV uninfected young adult will be included for comparison in physiopathological module (metabolic, cardiovascular, and immunological)
Intervention Type
Biological
Intervention Name(s)
blood sampling, specific biological exams and biobank and self administered questionnaires
Intervention Description
HIV INFECTION at inclusion and annually up to 06 years follow-up clinical and therapeutic evaluation by physician biological: blood sampling, specific biological exams and biobank self administered questionnaires In the physiopathological module: at inclusion and after 3 years follow up: OGTT, CT Scan, Dexa Scan, cardiovascular explorations (carotid intima media thickness, pulse wave velocity, transthoracic echocardiography) HIV UNINFECTED at inclusion and after 3 years follow up clinical evaluation by physician biological: blood sampling, specific biological exams and biobank self administered questionnaires
Primary Outcome Measure Information:
Title
Immuno virological and clinical prognosis: HIV RNA <50c/mL, CD4 cells count>500 cells/mL, vital status, CDC stage
Time Frame
at inclusion and annually up to 06 years follow-up
Secondary Outcome Measure Information:
Title
Professional and schooling integration, social life:marital status, type of accommodation, education level, type and age at first employment
Time Frame
at inclusion and annually up to 6 years follow up
Title
sexuality, sexual risk behaviour: age at first intercourse, condom use at first, last sexual intercourse, and during last year, unplanned pregnancy, interruption of pregnancy
Time Frame
at inclusion and annually up to 6 year follow-up
Title
metabolic and cardiovascular abnormalities: abnormalities in glucose tolerance and insulino-resistance, dyslipidemia, lipodystrophy, adipocyte dysfunction, atherosclerosis,dysfunction, median of intima media thickness and pulse wave velocity
Time Frame
at inclusion and after 3 years follow-up
Title
Lymphocyte phenotype and functional capacity of T lymphocyte: description of dysfunctional CMV-specific T cell, T cell responses measured at inclusion, and their evolution during follow-up
Time Frame
at inclusion and after 3 years follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Group of HIV Infection Inclusion Criteria: Age ≥ 18 and < 25 years Able to give written consent Covered by French Social Security diagnosis of HIV-1 et/ou-2 documented before age 13 Exclusion Criteria (for physiopathological module only) Under protection(saving) of justice Control Group Inclusion Criteria: Age ≥ 18 and ≤ 25 years Able to give written consent Covered by French Social Security With a brother or sister, cousin, father or mother HIV infected, inbred or adopted With a negative serology for HIV infection, HBV, HCV Without diabetes mellitus able to go to Clinical Investigation Center of Necker and to Hospital St. Antoine for the recruitment and monitoring Exclusion Criteria: Under protection(saving) of justice
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hugues Aumaitre
Organizational Affiliation
CH PERPIGNAN
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Eric Froguel
Organizational Affiliation
Hopital de Lagny
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michèle Bentata
Organizational Affiliation
Hopital Avicenne
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Philippe Genet
Organizational Affiliation
Hopital Argenteuil
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Olivier Patey
Organizational Affiliation
CHIC Villeneuve St Georges
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Laurence Gerard
Organizational Affiliation
St Louis Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Frédéric Lucht
Organizational Affiliation
St Etienne
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Bruno Hoen
Organizational Affiliation
St Jacques Besançon
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jean Luc Schmit
Organizational Affiliation
Hôpital Nord Amiens
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Claire Pintado
Organizational Affiliation
St Louis Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Cécile Goujard
Organizational Affiliation
Le Kremlin Bicetre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Thierry Allegre
Organizational Affiliation
CH Aix en Provence
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Alain Lafeuillade
Organizational Affiliation
CHIC Toulon
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Pierre De Truchis
Organizational Affiliation
Raymond Poincarré Garches
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Vincent Jeantils
Organizational Affiliation
Jean Verdier Bondy
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Claudine Duvivier
Organizational Affiliation
Institut Pasteur
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Laurence Slama
Organizational Affiliation
Tenon Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Olivier Bouchaud
Organizational Affiliation
Hopital Avicenne Bobigny
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marie Karmochkine
Organizational Affiliation
Georges Pompidou Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dominique Salmon Ceron
Organizational Affiliation
Cochin Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Emmanuel Mortier
Organizational Affiliation
Louis Mourier Colombes
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Roland Tubiana
Organizational Affiliation
Pitié Salpétrière Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Pierre Marie Girard
Organizational Affiliation
St Antoine Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
André Cabié
Organizational Affiliation
CHU Fort de France
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jean Marie Chennebault
Organizational Affiliation
University Hospital, Angers
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Philippe Morlat
Organizational Affiliation
St André Bordeaux
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Pierre Weinbreck
Organizational Affiliation
Hôpital Dupuytren
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Laurent Cotte
Organizational Affiliation
La Croix Rousse Lyon
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sophie Matheron
Organizational Affiliation
Bichat Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Véronique Reliquet
Organizational Affiliation
Hotel Dieu Nantes
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Philippe Pérré
Organizational Affiliation
CHD Les Oudairies La Roche Sur Yon
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Cédric Arvieux
Organizational Affiliation
Hopital Pontchaillou Rennes
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christine Cheneau
Organizational Affiliation
Centre Hospitalier Strasbourg
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Martine Obadia
Organizational Affiliation
CH Purpan Toulouse
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Renaud Verdon
Organizational Affiliation
CHU Cote de Nacre Caen
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christine Jacomet
Organizational Affiliation
Hopital Gabriel Montpied Clermont Ferrand
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lionel Piroth
Organizational Affiliation
CHU Hopital d'enfants Dijon
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Antoine Chéret
Organizational Affiliation
CH Tourcoing
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Yasmine Debab
Organizational Affiliation
CHU Charles Nicolle Rouen
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dominique Merrien
Organizational Affiliation
CH Compiègne
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Patrick Mercié
Organizational Affiliation
CHU St André Bordeaux
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Valérie Garrait
Organizational Affiliation
CHIC Créteil
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marie Aude Khuong
Organizational Affiliation
Centre Hospitalier Général St Denis
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Geneviève Beck Wirth
Organizational Affiliation
CH Mulhouse
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stéphane Blanche
Organizational Affiliation
Necker Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Franck Boccara
Organizational Affiliation
St Antoine Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Claudine Barbuat
Organizational Affiliation
CHR Caremeau Nimes
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jean Paul Viard
Organizational Affiliation
Hotel Dieu Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ghislaine Firtion
Organizational Affiliation
Cochin Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Albert Faye
Organizational Affiliation
Robert Debré Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Catherine Dollfus
Organizational Affiliation
Armand Trousseau Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Corinne Floch Tudal
Organizational Affiliation
Louis Mourier Colombes
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kamila Kebaili
Organizational Affiliation
Hopital de jour ISHOP Lyon
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Joelle Tricoire
Organizational Affiliation
CHU Paule de Viguier Toulouse
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Françoise Mazingue
Organizational Affiliation
CHR Jeanne de Flandres Lille
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Pascal Bolot
Organizational Affiliation
CHG St Denis
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Francois Bissuel
Organizational Affiliation
CH LC Fleming St Martin Guadeloupe
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anne Chace
Organizational Affiliation
CHIC Villeneuve St Georges
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Narcisse Elenga
Organizational Affiliation
CHG Andrée Rosemon Cayenne
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Natacha Entz Werle
Organizational Affiliation
Hautepierre Strasbourg
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Thomas Girard
Organizational Affiliation
Hotel Dieu Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Martine Levine
Organizational Affiliation
Robert Debré Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Benoit Martha
Organizational Affiliation
CH Chalon sur Soane
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sandrine Anne Martha
Organizational Affiliation
Chalon sur Saone
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Patrice Poubeau
Organizational Affiliation
CHR Réunion St Pierre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jean Marc Treluyer
Organizational Affiliation
CIC Necker Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Louis Bernard
Organizational Affiliation
Hôpital Bretonneau Tours
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michel Dupon
Organizational Affiliation
Hôpital Pellegrin Bordeaux
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
David Zucman
Organizational Affiliation
Hôpital Foch Suresnes
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anne Simon
Organizational Affiliation
Pitié Salpétrière Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Isabellle Poizot Martin
Organizational Affiliation
Ste Marguerite Marseille
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Thierry Prazuck
Organizational Affiliation
CHR Orléans
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Eric Doré
Organizational Affiliation
CHU Estains Clermont Ferrand
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Catherine Gaud
Organizational Affiliation
CHR Site Felix Guyon Bellepierre La Réunion
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpitaux (voir liste jointe)
City
De France
Country
France

12. IPD Sharing Statement

Links:
URL
http://anrs.fr
Description
Related Info

Learn more about this trial

Cohort of Young Adults Infected With HIV Since Birth or During Childhood

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