Can acupuncture shorten induced labor and ease pain?
NCT ID NCT07774442
First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time
Summary
This trial tests whether acupuncture can shorten the time from labor induction with a Cook's balloon to delivery, and whether it reduces pain and improves the experience. Pregnant women at 37 weeks or more who need induction will receive acupuncture at nine specific points. The study compares outcomes like time to delivery and pain scores to see if this complementary therapy offers benefits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Acupuncture therapy
- What this could lead to
- If effective, acupuncture could offer a drug-free way to shorten labor and reduce pain during induced labor, improving the birthing experience.
- What could go wrong
- This is a single-center trial with no prior studies on this specific use, so results may not be conclusive or widely applicable. Acupuncture is generally safe but may cause minor side effects like soreness or bruising.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- 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.
- 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: * pregnant woman with a gestational age of 37 weeks and above * age\>=18 years old * having medical indication to be labor induced by Cook's Balloon * speaking French * agreeing to participate by signing informed consent form Exclusion Criteria: * patient having contraindication for the use of Cook's balloon * patients under curatorship and/or guardianship
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CH de Roubaix
Roubaix, 59100, France
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Other studies related to the condition(s) this trial covers.
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