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Oxygen-Infused pads may ease Post-Birth pain for First-Time moms

NCT ID NCT07487974

Symptom relief Sponsor: KTO Karatay University Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Sep 02, 2026 · Updated 4 times

Summary

This study tested whether sanitary pads containing active oxygen and negative ions can reduce pain and improve healing after an episiotomy (a cut made during childbirth) in first-time mothers. 66 women were randomly assigned to use either the special pads or regular postpartum pads. Researchers measured pain, wound healing, and other physical symptoms in the days after birth to see if the special pads offered extra benefits.

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

66 people

The number who actually took part.

Started

Nov 2025

Finished

Dec 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: * Women aged 18 years or older * At least primary school education * Gestational age between 37 and 42 weeks * Single, live, vaginal birth * Mediolateral episiotomy performed * Hemoglobin level \> 11 mg/dL * Voluntary participation and ability to provide informed consent Exclusion Criteria: * History of high-risk pregnancy * History of high-risk or complicated labor * Use of operative vaginal delivery methods (forceps, vacuum, etc.) * Presence of additional perineal lacerations, including 3rd-degree tears or anal sphincter injury * Cephalopelvic disproportion * Postpartum hemorrhage * Newborn requiring NICU care * Diagnosis of vaginal fungal infection or sexually transmitted infections (e.g., herpes simplex, HPV)

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Conditions

The condition(s) this trial relates to.

Pain puerperal disorder

As listed by the trial registrant

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

Episiotomy Episiotomy wound Postpartum complication Postpartum recovery Primiparous women

Contacts and locations

Locations

  • Eğitim ve Araştırma Hastanesi

    Karaman, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.