Which late abortion method causes less anxiety? a new study investigates
NCT ID NCT06140069
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
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Dec 2024
- Finished
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Dec 2024
- Lead sponsor
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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
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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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 Hide 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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