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Osteopathic touch eases constipation in small trial

NCT ID NCT06196073

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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested a hands-on therapy called visceral osteopathy for people with functional constipation. 27 adults received either osteopathic manual therapy or standard dietary advice. The goal was to see if the manual therapy could improve bowel symptoms and quality of life better than conventional methods.

What this could mean

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

Active substance
osteopathic manual therapy
What this could lead to
If it works, this could offer a non-drug, hands-on option to ease constipation symptoms and improve quality of life.
What could go wrong
This is a small, completed trial with only 27 participants, so results may not apply to everyone. The therapy is manual and effects can 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

27 people

The number who actually took part.

Started

Oct 2023

Finished

Nov 2024

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

Anyone

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: * Volunteer individuals aged 18 and over * Clinical diagnosis with functional constipation based on ROMA IV criteria Exclusion Criteria: * Clinical diagnosis of a gastrointestinal disease other than constipation, * Undergone abdominal surgery in the last 6 months, * Having abdominal aortic aneurysm, acute rectal bleeding, malignant mass in the GIS, * Pregnancy or suspected of pregnancy, * Cliniclal diagnosis of neurological disease that may cause constipation, * Expreinced unexplained fever, Individuals with night sweats and weight loss

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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.

Contacts and locations

Locations

  • Pamukkale University

    Denizli, Pamukkale, 20000, Turkey (Türkiye)

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