Requests for Medical Termination of Pregnancy for Psychological or Social Maternal Reasons

NCT05499325 | Unknown

• 1 other identifier: CHSD_0028_MATER
• Study Type: observational
• Target: 120
• Locations: 1 country
• Sites: 1

Brief Summary

When the request for termination of pregnancy is made at a term of less than sixteen weeks of amenorrhea, the patients have complete decision-making autonomy. This is called voluntary termination of pregnancy. On the other hand, when they are made after this term, their requests must be subject to a multidisciplinary assessment. This is called medical termination of pregnancy for maternal indication. Schematically, there are two categories of indications: "organic" (progressive cancer, severe heart disease, etc.) and "psycho-social". In the latter case, and although the recommendations of the CNGOF recommend a formalization of these requests in the centers where the patients are received, strong disparities are observed in practice. In addition, there are few epidemiological and clinical data concerning these medical terminations of pregnancy with a psychological or social maternal indication in the literature. The objective of this work is to describe the demographic characteristics of patients who have made a request for termination of pregnancy after the legal deadline for psychological or social maternal reasons, and to specify the care pathways of these patients.

Conditions

Pregnancy Related

Keywords

Medical termination of pregnancy; Psychic or social reason

Outcome Measures

Primary Outcomes (9)

• age

  epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons

  Day 1

• place of life

  epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons

  Day 1

• social security

  epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons

  Day 1

• level of studies

  epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons

  Day 1

• occupation / resources

  epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons

  Day 1

• marital status

  epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons

  Day 1

• number of children

  epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons

  Day 1

• native country

  epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons

  Day 1

• recent life events

  epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons

  Day 1

Secondary Outcomes (3)

• migratory route

  Day 1

• medical and surgical history

  Day 1

• gynecological follow-up, and follow-up of the current pregnancy

  Day 1

Eligibility Criteria

• Sex: female
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients followed at the Maison des Femmes, having consulted between 01/01/2016 and 02/28/2022, having undergone a medical termination of pregnancy for psychological or social maternal reasons

You may qualify if:

• Minor or adult patients who have been seen at the Maison des Femmes in the context of a request for termination of pregnancy for psychological and/or social maternal reasons, including patients subject to a legal protection measure (guardianship , curators) during the consultation
• Consultation between 01/01/2016 and 02/28/2022

You may not qualify if:

• Objection to the use of data or refusal to participate (patient or guardian)

Sponsors & Collaborators

• Centre Hospitalier de Saint-Denis: lead

Study Sites (1)

Hôpital DELAFONTAINE

Saint-Denis, Île-de-France Region, 93200, France

Location

Related Links

• Women victims of violence

Central Study Contacts

Anne BEDU, JD

CONTACT

01.42.35.61.28; annebedu.ab@gmail.com

Tiphaine DE FOUCHER DE CAREIL, MD

CONTACT

01.42.35.61.28; tiphaine.defoucherdecareil@ch-stdenis.fr

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: RETROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 11, 2022
• First Posted: August 12, 2022
• Study Start: August 17, 2022
• Primary Completion: August 17, 2022
• Study Completion: November 30, 2022
• Last Updated: August 12, 2022

Record last verified: 2022-08

Locations

FR (1)