Ear acupressure eases Post-Birth pain, study finds

NCT ID NCT07277478

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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 Results may not be published yet.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)

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Not a trial. The treatment could once be requested outside a study, but no longer can.
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The treatment has been approved, so it is available normally rather than through this programme.

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Status unknown
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First seen Jun 27, 2026 ยท Last updated Jun 27, 2026

Summary

This study tested whether placing small magnetic beads on specific points of the ear (auricular acupressure) could help reduce pain in women who had an episiotomy during childbirth. 86 women participated, with half receiving the real treatment and half receiving a placebo. The results showed that the treatment may help lower pain and improve satisfaction with pain care.

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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

90 people

The number who actually took part.

Started

Dec 2024

Finished

Sep 2025

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

Accepted

You do not need to have the condition being studied to take part.

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- 1. Women with singleton pregnancies who delivered vaginally. 2. Women who underwent episiotomy. 3. Gestational age between 37 and 42 weeks. 4. Willing to participate in the study and provide signed informed consent. 5. Age 18 years or older. -Exclusion Criteria- 1. Women with skin lesions or allergies at the auricular acupressure site. 2. Women with gynecological disorders, such as uterine fibroids, adenomyosis, or endometriosis. 3. Women or newborns with severe postpartum complications, such as postpartum hemorrhage, infection, perineal hematoma, major neonatal diseases, or admission to the neonatal intensive care unit. 4. Women with psychiatric disorders, such as anxiety or depression.

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Conditions

The condition(s) this trial relates to.

Pain

As listed by the trial registrant

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

Contacts and locations

Locations

  • Hsiao Ai Wen

    Taipei, Sanchong, 241, Taiwan

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