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New pain block could speed recovery after belly surgery

NCT ID NCT07586462

Knowledge-focused Sponsor: San Giovanni di Dio Hospital 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study looks at whether a Deep Rectus Sheath (Preperitoneal) block helps people recover better after abdominal surgery. About 60 adults having open or laparoscopic abdominal surgery will receive standard pain management, which may include this block or other nerve blocks. Researchers will measure pain scores, recovery quality, and how quickly patients get back on their feet.

What this could mean

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

Active substance
Deep Rectus Sheath (Preperitoneal) block
What this could lead to
If effective, this block could become a standard option for better pain control and faster recovery after abdominal surgery.
What could go wrong
This is a small observational study, not a randomized trial, so results may be influenced by patient selection and cannot prove cause and effect.

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 60 people

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

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

May 2027

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.

Who is studied

Patients undergoing abdominal surgery, either open or laparoscopic

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: * Age ≥ 18 years * Patients undergoing abdominal surgery, either open or laparoscopic * ASA physical status I-III * Neuraxial or general anesthesia according to standard clinical practice * Provision of informed consent to participate in the study Exclusion Criteria: * Refusal to provide informed consent * Contraindications to locoregional anesthesia * Known allergy to local anesthetic agents * Coagulation disorders or incompatible anticoagulant therapy * Infection at the injection site * Cognitive impairment preventing reliable assessment of outcomes

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As listed by the trial registrant

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

Abdominal surgery by laparotomy Laparoscopy

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

  • Crotone Hospital

    NOT_YET_RECRUITING

    Crotone, Italy

  • Crotone Hospital

    RECRUITING

    Crotone, Italy

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