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Nationwide study reveals how labor induction methods affect mothers and babies

NCT ID NCT02477085

Knowledge-focused Sponsor: Assistance Publique - Hôpitaux de Paris 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 completed French study looked at over 3,000 women whose labor was started artificially (induced). Researchers compared different methods like breaking the water, using hormones, or a balloon catheter. They tracked how often each method was used, how it affected the mother and baby, and whether women were satisfied. This is an observational study, not a test of a new drug or treatment.

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

3,049 people

The number who actually took part.

Start date

Nov 2015

Finished

Dec 2016

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

all women who have an induced labor

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: * patient who has a labor induction * with a live fetus at the beginning of induction * patient who did not have any opposition to use her medical and personal data or her child's medical data for research Exclusion Criteria: * in utero fetal death * termination of pregnancy * patient's refusal to participate to the study

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As listed by the trial registrant

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

Induction of labor

Contacts and locations

Locations

  • Port-Royal maternity unit, Cochin Hospital, Assistance publique des Hôpitaux de Paris (APHP

    Paris, 75014, France

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