Abortions at Strasbourg University Hospitals

September 20, 2019 updated by: University Hospital, Strasbourg, France

A Survey of Best Practices of Abortions at Strasbourg University Hospitals

The number of abortions in France and Strasbourg has been stable for several years. In 2017, 1847 were performed in the Gynecology-Obstetrics Department for 6146 deliveries (23% of all pregnancies). It therefore seems important to evaluate the professional practices, but also the experiences of the patients.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Anticipated)

2000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • France
      • Strasbourg, France, 67098
        • Les Hôpitaux Universitaires de Strasbourg
        • Sub-Investigator:
          • Philippe DERUELLE
        • Sub-Investigator:
          • Romain FAVRE
        • Contact:
        • Principal Investigator:
          • Antoine KOCH
        • Sub-Investigator:
          • Karima BETTAHAR
        • Sub-Investigator:
          • Thomas BOISRAME

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Patient in the first trimester of pregnancy wishing an abortion

Description

Inclusion criteria:

  • Patient in the first trimester of pregnancy wishing an abortion
  • Age: greater than or equal to 18 years.
  • Patient affiliated to a social security system

Exclusion criteria:

  • Patient after the first trimester pregnancy
  • Patient benefiting from a legal protection measure
  • Bad understanding of French.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Request for abortion
Patient in first trimester of pregnancy in request for abortion
Procedure: Evaluation of the procedure of abortion
Observational study using questionnaires

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluate the investigator's professional practices regarding abortion, particularly in relation to the recommendations for clinical practice of the National College of French Obstetricians Gynecologists (CNGOF) published in 2016.
Time Frame: 6 weeks
The patients will complete a questionnaire
6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of the sociological, economic and psychological factors motivating the request for abortion
Time Frame: 6 weeks
The patients will complete a questionnaire
6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University Hospital, Strasbourg, France

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

September 1, 2019

Primary Completion (Anticipated)

September 1, 2019

Study Completion (Anticipated)

October 1, 2020

Study Registration Dates

First Submitted

July 4, 2019

First Submitted That Met QC Criteria

September 20, 2019

First Posted (Actual)

September 24, 2019

Study Record Updates

Last Update Posted (Actual)

September 24, 2019

Last Update Submitted That Met QC Criteria

September 20, 2019

Last Verified

July 1, 2019

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 7472

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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