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New study aims to find best pain relief for robotic prostate surgery patients

NCT ID NCT07483840

Symptom relief Sponsor: Ente Ospedaliero Ospedali Galliera Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study tests three different pain-blocking methods in 147 men having robotic prostate surgery. The goal is to see which method provides the best pain relief, reduces the need for strong painkillers, and helps patients recover faster. Participants will receive one of three techniques: a back muscle block, a belly muscle block, or a low-dose spinal injection.

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 147 people

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

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Dec 2028

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

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

Sex

Male 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 patients scheduled for elective robot-assisted radical prostatectomy or robot-assisted simple prostatectomy * Presence of a clinical indication for robot-assisted prostate surgery * American Society of Anesthesiologists (ASA) physical status ≥ II * Ability to understand the study procedures and provide written informed consent * Agreement to participate in the study and compliance with study procedures Exclusion Criteria: * Patients undergoing open (laparotomic) or emergency surgery Contraindications to central or loco-regional anesthesia techniques, including but not limited to: * Coagulation disorders or ongoing anticoagulation incompatible with neuraxial or regional anesthesia * Known allergy or hypersensitivity to local anesthetics or study drugs * Severe spinal deformities * Severe aortic stenosis * Systemic sepsis or infection at the site of needle insertion Refusal or inability to provide informed consent

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As listed by the trial registrant

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

Postoperative analgesia

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

  • Galliera Hospital

    Genova, Ge, 16128, Italy

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