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Which late abortion method causes less anxiety? a new study investigates

NCT ID NCT06140069

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
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 Results may not be published yet.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 This study
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This status has not been confirmed recently, so it may be out of date.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 Jul 21, 2026 · Last updated Jul 22, 2026 · Updated 1 time

Summary

This study looks at women undergoing abortion between 14 and 16 weeks of pregnancy, comparing those who choose a surgical method (a quick procedure in the operating room) with those who choose a medical method (taking medication to end the pregnancy over several hours). Researchers want to see if one method is linked to more anxiety or depression afterward. The goal is to help doctors give better information so women can make an informed choice.

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 this study yields clear findings, it could help clinics offer better, more personalized guidance to women choosing between surgical and medical late abortion.
What could go wrong
This is an observational questionnaire study, not a controlled trial, so it cannot prove cause and effect. Results may be influenced by patient self-selection and other unmeasured factors.

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.

Started

Dec 2024

Finished

Dec 2024

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 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: * Any adult patient * Having given her non-opposition after clear and fair information (patient who understands and reads French) * Patient treated at the Toulouse University Hospital for an abortion between 14 and 16 weeks (dating by ultrasound) * Singleton pregnancy * Progressive pregnancy Exclusion Criteria: * Protected adult patient (guardianship, curatorship, protection of justice) * Developing psychiatric pathologies * Fetal anomaly detected

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As listed by the trial registrant

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

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