Acupuncture needles to kickstart labor? tiny study investigates
NCT ID NCT06357962
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study tested whether semi-permanent acupuncture could reduce the need for medical induction of labor in pregnant women at low or moderate risk. Only 8 women participated before the trial was terminated early. The goal was to see if this approach is feasible and to plan a larger study, but no firm conclusions can be drawn from such a small sample.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- semi-permanent acupuncture
- What this could lead to
- If it works, this could point toward a non-drug way to help labor start naturally, reducing the need for medical induction.
- What could go wrong
- This was a tiny pilot study with only 8 participants and was terminated early. The results are too small to draw any conclusions, and acupuncture may not work for everyone.
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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8 people
The number who actually took part.
- Started
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May 2024
- Finished
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Apr 2025
- 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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Up to 40 years
- 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: * Anticipated delivery at the study center. * Ability to collaborate in necessary evaluations. * Legal capacity to provide informed consent. * Signature of the informed consent for inclusion in the study, by oneself. Exclusion Criteria: * Pregnancy with high or very high risk as described by the Pregnancy and Childbirth Monitoring Protocols of the Department of Health of Catalonia * History of cesarean delivery. * Language barrier preventing collaboration in study procedures. * Cognitive or affective pathology limiting the ability to collaborate with study procedures. * Participation in another clinical trial involving an experimental intervention during the period of this trial and/or establishing a visit frequency incompatible with this trial.
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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.
Contacts and locations
Locations
-
Consorci Sanitari Alt Penedes i Garraf
Vilafranca del Penedès, Barcelona, 08720, Spain
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