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Light therapy eases Post-Birth pain and speeds healing, study finds

NCT ID NCT06893315

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study looked at whether photobiomodulation (PBM) therapy, a type of light treatment, can reduce pain and improve healing for women who had perineal tears or cuts during vaginal birth. 183 women were offered PBM in addition to standard care. Researchers compared pain scores and healing in those who accepted PBM versus those who declined. The goal was to see if adding light therapy helps more than standard treatments alone.

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.

Participants

183 people

The number who actually took part.

Started

Sep 2024

Finished

Jun 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.

Who is studied

Patients undergoing episiotomy or patients who presented grade 2 or 3 perineal laceration during vaginal childbirth. The diagnosis of the degree of laceration is clinical and the obstetrician responsible for the patient's care treatment did so by exploring the injury and visualizing the injured structures within the hospital's care routine. Only those patients in whom the diagnosis of grade 2 or 3 perineal laceration made by the responsible care team and documented in the medical record were invited to participate in the study.

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: * Adult women over 18 years of age; * Parturients with a gestational age equal to or greater than 37 weeks; * Patients who had a vaginal birth; * Patients undergoing episiotomy or patients who presented grade 2 or 3 perineal laceration during childbirth. Exclusion Criteria: * Multiple pregnancy (twins); * Presence of fetal malformation or death identified during prenatal care or at the time of hospitalization for delivery; * Patients with serious complications such as severe puerperal hemorrhage or HELLP Syndrome during childbirth. * Patients with grade 1 or 4 perineal lacerations. * Presence of systemic diseases that alter the repair process. * Withdrawal of the nformed Consent Form" (ICF) at the request of the patient or those responsible;

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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

  • Hospital Universitário Materno-Infantil da Universidade Estadual de Ponta Grossa

    Ponta Grossa, Paraná, 05020000, Brazil

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