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Recruiting NCT06666530

NCT06666530 Quality of Life Related to the Care of Women Living With HIV During the Perinatal Period

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Clinical Trial Summary
NCT ID NCT06666530
Status Recruiting
Phase
Sponsor Assistance Publique - Hôpitaux de Paris
Condition HIV
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2024-06-19
Primary Completion 2027-12

Trial Parameters

Condition HIV
Sponsor Assistance Publique - Hôpitaux de Paris
Study Type OBSERVATIONAL
Phase N/A
Enrollment 100
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2024-06-19
Completion 2027-12
Interventions
Questionary

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Brief Summary

"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."

Eligibility Criteria

"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 Exclusion Criteria * Refusal to participate in the study * Non-French speaker"

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