Acupressure may offer drug-free relief after cesarean birth

NCT ID NCT07805720

What the study statuses mean

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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 Results may not be published yet.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
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Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

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

60 people

The number who actually took part.

Started

Apr 2026

Finished

May 2026

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.

Ages

18 years and older

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: * 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.

anxiety disorder Pain, Postoperative

As listed by the trial registrant

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

Contacts and locations

Locations

  • Tien Giang Obstetrics and Gynecology Hospital

    Mỹ Tho, Tien Giang, Vietnam

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