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Immunology of the Infection Perinatal

NCT01055873 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 93

Last updated 2010-11-18

No results posted yet for this study

Summary

ANRS-EP38-IMMIP is a non interventional study. A single blood sample (30 mL) was drawn during a hospital visit for clinical follow-up. Immunological assays were performed on fresh blood. Cells and plasma were stored and kept frozen for additional biological evaluations.

Patients are included in the French perinatal cohort (ANRS CO-10), or have been followed since before 1996 in the same clinical sites as patients who belong to ANRS CO-10. In the ANRS CO-10 cohort, all patients are prospectively followed from birth.

Conditions

  • HIV Infections

Interventions

BIOLOGICAL

A single blood sample (30 mL)

A single blood sample (30 mL) was drawn during a hospital visit for clinical follow-up. Immunological assays were performed on fresh blood. Cells and plasma were stored and kept frozen for additional biological evaluations

Sponsors & Collaborators

  • Institut Pasteur

    collaborator INDUSTRY

  • University of Paris 5 - Rene Descartes

    collaborator OTHER

  • Hôpital Necker-Enfants Malades

    collaborator OTHER

  • French National Agency for Research on AIDS and Viral Hepatitis

    lead OTHER_GOV

Principal Investigators

  • Warszawski MD Josiane, Methodologist · INSERM U 822, Hôpital de Bicêtre, portes 10 à 15, 82 rue du Général Leclerc, 94276 Le Kremlin-Bicêtre Cedex [email protected] ; Tel : 01 45 21 22 86

  • Blanche PHD Stéphane · Hopital Necker Enfants malades-Service immunologie hématologie pédiatrique -149 rue de Sèvres- 75015 PARIS 01 44 49 48 24

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-02-28
Primary Completion
2009-02-28
Completion
2009-02-28

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01055873 on ClinicalTrials.gov