Acupressure may offer drug-free relief after cesarean birth
NCT ID NCT07805720
First seen Sep 04, 2026 · Last updated Sep 04, 2026
Summary
This trial tests whether acupressure, a traditional therapy that presses on specific body points, can reduce pain and anxiety in women who have just had a cesarean delivery. Sixty postpartum women will receive either acupressure or a sham version, along with standard medical care, for three days. Researchers will measure pain and anxiety levels before and after the treatment to see if acupressure adds any benefit beyond usual care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Acupressure, a manual therapy applying pressure to specific body points
- What this could lead to
- If acupressure works, it could offer a drug-free way to ease pain and anxiety after cesarean delivery, reducing reliance on painkillers.
- What could go wrong
- This is a small early trial, and the sham comparison may not fully mask the effect. Results may not apply to all postpartum women.
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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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60 people
The number who actually took part.
- Started
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Apr 2026
- Finished
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May 2026
- 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: * Postpartum women aged 18 years or older who have undergone cesarean delivery with spinal anesthesia. * Gestational age \>= 37 weeks. * Willing to participate and signing the written informed consent form. Exclusion Criteria: * General anesthesia or methods other than spinal anesthesia. * Hearing, vision, or speech impairment. * History of chronic diseases such as uncontrolled diabetes, severe hypertension, cardiovascular disease, or psychiatric disorders. * Diagnosed with chronic pain before surgery, or regular use of pain medications. * Opioid, alcohol addiction or dependence. * Pathological cesarean deliveries (placenta praevia, placental abruption, placenta accreta). * Multiple pregnancies (twins, triplets, etc.). * Post-operative complications (wound infection, hemorrhage, coagulation disorders, or loss of the child). * Severe postpartum urinary retention requiring urinary catheterization. * Refusing to participate.
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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
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Tien Giang Obstetrics and Gynecology Hospital
Mỹ Tho, Tien Giang, Vietnam
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