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NCT06666530Recruiting

Quality of Life Related to the Care of Women Living With HIV During the Perinatal Period

Source: ClinicalTrials.gov · Last updated 8 Jan 2026

Brief summary (registry, in English)

"The improvement of patient care by assessing the Quality of Life Related to Care (QLRC) in pregnant women living with HIV is of great importance for informing decision-making, resource allocation, and health policy formulation Prospective descriptive survey of women living with HIV followed for a pregnancy in the Infectious diseases department of Bichat-Claude Bernard Hospital, PARIS, France, between the first obstetric ultrasound and the 28th week of amenorrhea. After recruitment during a follow-up consultation: Information regarding the prenatal and perinatal management of HIV and the infant's outcomes up to 12 months will be collected retrospectively through the medical records. Three self-questionnaires, either completed independently or with assistance, will be administered at inclusion (between the first obstetric ultrasound and 28 weeks of amenorrhea), during the third trimester of pregnancy, and at 1 year postpartum."

Status (registry)
Recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
21 Oct 2024
Start date
19 Jun 2024
Primary completion date
Dec 2027
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Diseases
HIV
NCT number
NCT06666530

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From 19 Jun 2024 to the primary completion date, Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Refusal to participate in the study
  • Non-French speaker"

Criteria the registry did not label

  • "Inclusion Criteria
  • Woman living with HIV
  • Age ≥ 18 years
  • Pregnant - due date between the first obstetric ultrasound and 28 weeks of amenorrhea
  • Information provided about the study and the right to refuse participation

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Hôpital Bichat - Claude-Bernard
Coordinator of this site? Confirm its status
ParisFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.