Ear seeds may ease C-Section pain without drugs
NCT ID NCT07322601
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether placing small seeds on specific ear points (auricular acupressure) can reduce pain after a cesarean section. Seventy women were randomly assigned to receive either real acupressure or a sham (fake) version. Their pain levels and use of painkillers were tracked for 48 hours after surgery. The goal was to see if this simple, non-invasive technique could help manage post-surgical pain.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- auricular acupressure (vaccaria seeds applied to ear points)
- What this could lead to
- If it works, this could offer a simple, drug-free way to ease pain after C-section and reduce the need for painkillers.
- What could go wrong
- This is a small, single study. The effect may be small or due to a placebo effect, and results may not apply to all women or settings.
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
-
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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70 people
The number who actually took part.
- Started
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Oct 2024
- Finished
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Jun 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
-
18 to 40 years
- Sex
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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 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: * 18-40 years of age * Gestational age ≥ 37 weeks * Alert and cooperative with the treating physicians * Able to understand and use the Visual Analog Scale (VAS) * Preoperative American Society of Anesthesiologists (ASA) Physical Status Classification System I-II * Anesthesia: spinal anesthesia; * Pfannenstiel suprapubic transverse incision * Infant 5-minute Appearance, Pulse, Grimace, Activity, Respiration score (Apgar score) \> 7 * Cesarean operative time ≤ 60 minutes * Singleton pregnancy * Voluntary agreement to participate. Exclusion Criteria: * Contraindication to diclofenac * Surgical complications, including hysterectomy and postpartum hemorrhage (\> 1000 ml) * History of acupuncture syncope * Preoperative chronic pain and/or regular preoperative use of analgesics * Addiction to or dependence on opioids or alcohol * Diabetes mellitus or HIV infection * Prior Auricular acupressure * Skin lesions of the auricle * Surgical wound infection
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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
-
Le Van Thinh Hospital
Ho Chi Minh City, Binh Trung Ward, Vietnam
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