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Can light therapy ease a hidden digestive struggle?

NCT ID NCT07771218

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 18, 2026 · Last updated Aug 19, 2026 · Updated 1 time

Summary

This trial tests whether adding low-level laser therapy to a standard program of diet changes and biofeedback training can help women with obstructive defecation syndrome (ODS), a condition that makes it hard to empty the bowels. Women aged 30-45 with ODS will be randomly assigned to receive either standard care alone or standard care plus laser therapy on the lower back. The study will measure changes in symptom severity, anorectal function, and quality of life to see if the laser adds meaningful benefit.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
low-level laser therapy (LLLT) applied to the lumbosacral region, added to nutritional modification and biofeedback training
What this could lead to
If effective, adding low-level laser therapy to standard care could offer a non-invasive way to ease symptoms and improve quality of life for women with obstructive defecation syndrome.
What could go wrong
This is a small early-stage trial, so results may not apply broadly. The laser's benefit over standard care alone is unproven, and individual responses may vary.

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

About 40 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Aug 2026

An estimate. Start dates often move.

Expected to finish

Dec 2026

An estimate. End dates often move.

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

30 to 45 years

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: * Woman diagnosed with ODS according to the Renzi ODS score (≥ 9). * They suffer from difficult defecation for at least three months. * Their ages will range from 30-45 years old. * Their body mass index (BMI) will range from 25-30 kg/m2. * Their parity number will be 2-3 times. Exclusion Criteria: * Any abnormalities around cancer colon, interstitial cystitis, or endometriosis. * Enlarged rectal diameter and damaged mienteric plexus and abnormal motor function of rectum. * Psychological or mental health problems. * Pregnancy and lactation * A history of previous pelvic surgery. * A history of retinopathy.

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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.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Faculty of Physical Therapy, Cairo University

    Giza, Egypt

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