- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05499325
Requests for Medical Termination of Pregnancy for Psychological or Social Maternal Reasons
Requests for Medical Termination of Pregnancy for Psychological or Social Maternal Reasons at the "Maison Des Femmes" in Saint-Denis : Retrospective Study Between 2016 and 2022
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.
Study Overview
Status
Conditions
Detailed Description
Retrospective cohort (from 01/01/2016 to 02/28/2022) single-centre involving data from patients followed at the Maison des Femmes, and eligible for the study.
The demographic and care pathway variables will be the subject of a descriptive statistical analysis.
Expected results: improvement of knowledge relating to patients who consulted for termination of pregnancy after sixteen weeks of amenorrhea and their care pathway.
Outlook:
- Improving the knowledge of health professionals and therefore of care pathways, with a view to a more homogeneous use of legal systems.
- Improvement and simplification of care pathways.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Anne BEDU, JD
- Phone Number: 01.42.35.61.28
- Email: annebedu.ab@gmail.com
Study Contact Backup
- Name: Tiphaine DE FOUCHER DE CAREIL, MD
- Phone Number: 01.42.35.61.28
- Email: tiphaine.defoucherdecareil@ch-stdenis.fr
Study Locations
-
-
Ile De France
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Saint-denis, Ile De France, France, 93200
- Hôpital Delafontaine
-
Contact:
- Stéphanie COSSEC
- Phone Number: 6962 01 42 35 61 40
- Email: coordination.rechercheclinique@ghtpdfr.fr
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Principal Investigator:
- Anne BEDU, JD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- Refusal of inclusion in a study explained in the medical file (patient or guardian)
- Objection to the use of data or refusal to participate (patient or guardian)
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
age
Time Frame: Day 1
|
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
place of life
Time Frame: Day 1
|
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
social security
Time Frame: Day 1
|
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
level of studies
Time Frame: Day 1
|
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
occupation / resources
Time Frame: Day 1
|
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
marital status
Time Frame: Day 1
|
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
number of children
Time Frame: Day 1
|
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
native country
Time Frame: Day 1
|
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
recent life events
Time Frame: Day 1
|
epidemiology of patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
migratory route
Time Frame: Day 1
|
care pathway for patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
medical and surgical history
Time Frame: Day 1
|
care pathway for patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
gynecological follow-up, and follow-up of the current pregnancy
Time Frame: Day 1
|
care pathway for patients who have undergone medical termination of pregnancy for psychological or social maternal reasons
|
Day 1
|
Collaborators and Investigators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- CHSD_0028_MATER
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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