- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07335939
Late-term Abortions Between 14 and 16 Weeks of Gestation: Comparison of Hemorrhagic Risks in Surgical vs. Medical Abortions (IVG-Tardives)
January 2, 2026 updated by: University Hospital, Strasbourg, France
Since the extension of the legal abortion limit to 16 weeks by the law of March 2, 2022, we must adapt our care to reduce the risks associated with this procedure.
According to the French National Authority for Health (HAS), all abortions after 9 weeks of gestation should be performed surgically, but the French National College of Gynecologists and Obstetricians (CNGOF) indicates that each patient should have the choice of method regardless of the gestational age at the time of the abortion.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
50
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
- Name: Victor Gabrielle, MD
- Phone Number: 33 3 69 55 34 04
- Email: Victor.gabriele@chru-strasbourg.fr
Study Locations
-
-
-
Strasbourg, France, 67091
- Recruiting
- Service de Gynécologie-Obstétrique - CHU de Strasbourg - France
-
Contact:
- Victor Gabriele, MD
- Phone Number: 33 3 69 55 34 04
- Email: Victor.gabriele@chru-strasbourg.fr
-
Principal Investigator:
- Victor Gabriele, MD
-
Sub-Investigator:
- Charlotte BORDES, MD
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Sub-Investigator:
- Georges Emmanuel ROTH
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-
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
- Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
- Adult woman with single or multiple pregnancy and undergoing an abortion between 14 and 16 weeks of gestation at the Strasbourg University Hospital between March 2, 2022, and March 2, 2026
Description
Inclusion Criteria:
- Adult woman
- Single or multiple pregnancy
- Undergoing an abortion between 14 and 16 weeks of gestation at the Strasbourg University Hospital between March 2, 2022, and March 2, 2026
Exclusion Criteria:
- Missed Pregnancy
- Term < 14 Weeks of Gestation or > 16 Weeks of Gestation
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Bleeding (in cc)
Time Frame: During surgery
|
Bleeding > 500 cc means a very large blood loss
|
During surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
May 19, 2025
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
June 19, 2026
Study Registration Dates
First Submitted
January 2, 2026
First Submitted That Met QC Criteria
January 2, 2026
First Posted (Actual)
January 13, 2026
Study Record Updates
Last Update Posted (Actual)
January 13, 2026
Last Update Submitted That Met QC Criteria
January 2, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 9690
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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