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New study examines safety of later surgical abortions

NCT ID NCT06396338

Knowledge-focused Sponsor: University Hospital, Toulouse Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 312 women who had surgical abortions between 10 and 16 weeks of pregnancy. Researchers compared bleeding risks between those who had the procedure at 10-14 weeks versus 14-16 weeks. Participants also filled out questionnaires about anxiety and depression. The goal is to improve information for patients and doctors about the safety of later abortions.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this study could provide better safety data to help patients and doctors make informed choices about late surgical abortions.
What could go wrong
This is a completed observational study with 312 participants, so results are limited in size and may not apply to all populations. No new treatment is being tested.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

312 people

The number who actually took part.

Started

Jul 2024

Finished

Feb 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Patient coming at hospital for voluntary termination of pregnancy (abortion)

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Woman treated for the performance of a surgical abortion between 10 and 16 weeks (dating by ultrasound) * Singleton pregnancy Exclusion Criteria: * Protected adult patient (guardianship, curatorship, safeguard of justice) * Refusal to participate expressed by the patient

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Voluntary termination of pregnancy

Contacts and locations

Locations

  • CHU Toulouse

    Toulouse, France

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