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Breaking wind, breaking ground: new study links Post-Surgery gas to recovery

NCT ID NCT06675097

Knowledge-focused Sponsor: University Hospital, Angers Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 11, 2026 · Updated 2 times

Summary

This study looks at whether the amount and type of gas a person passes after abdominal surgery can help predict complications. Researchers will track 200 adults before and after surgery, asking them to record details about their gas. The goal is to see if gas quality can serve as an early warning sign for problems, potentially leading to a simple, non-invasive tool to improve recovery monitoring.

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

About 200 people

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

Started

Jan 2025

Expected to finish

Apr 2027

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The patients will be included in the hospital they will be operated on

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: * Patients ≥18 years old * Indication for open or laparoscopic abdominal surgery * Whose expected length of stay is ≥ 2 days Non Inclusion Criteria: * Patients requiring a stomy on the initial surgery * Emergency surgery * Patient not knowing how to read or write * Poor understanding of the French language * Person deprived of liberty by judicial or administrative decision * Person subject to psychiatric care under duress * Person subject to a legal protection measure * Person unable to express consent * Person objecting to participating in research Exclusion Criteria: -Immediate post-operative intensive care with patient intubation

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Conditions

The condition(s) this trial relates to.

Mucopolysaccharidosis IV Postoperative Complications

As listed by the trial registrant

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

Postoperative complication Recovery, physiological

How to take part

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

  1. The places running it

    2 sites. 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

  • Angers Hospital (visceral surgery department)

    RECRUITING

    Angers, 49933, France

  • University Hospital of Nantes, CIC Institut des Maladies de l'appareil digestif, CHU Nantes, 1 place Alexis Ricordeau 44093 Nantes cedex 01

    RECRUITING

    Nantes, Loire Atlantique, 44093, France

More trials for these conditions

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