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New study aims to find best painkiller for C-Section recovery

NCT ID NCT07377630

Symptom relief Sponsor: Istituto Giannina Gaslini 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compares two ways to manage pain after a planned C-section: a small dose of morphine given with the spinal anesthesia, versus a nerve block (TAP block) using numbing medicine. One hundred women will be randomly assigned to one of the two groups. The goal is to see which method provides better pain relief and fewer side effects for the mother and baby.

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

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

About 100 people

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

Expected to start

Mar 2026

An estimate. Start dates often move.

Expected to finish

Mar 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.

Ages

18 years and older

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: * Planned for elective Cesarean Section (CS) * Scheduled for spinal anesthesia * Gestational age \> 34 weeks * Age 18 years or above * Ability to read and understand the information sheet and to sign and date the consent form Exclusion Criteria: * American Society of Anesthesiologists (ASA) classification \>2 * Body Mass Index (BMI) ≥ 40 kg/m2 * Weight \< 50 kg * Height \< 150 cm or ≥ 180 cm * Complicated Pregnancy (abnormal placentation, preeclampsia or others) * Women with opioid use disorder * Contraindication to spinal anesthesia (clotting disorder, local infection, spinal malformation, elevated intracranial pressure) * Contraindication to Transabdominal Plane Block (TAP) block (skin infection, abdominal wall muscle defects) * Allergy/contraindication to any medication used in the study * Previous median abdominal incision * Emergency or unplanned CS

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As listed by the trial registrant

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

Cesarean section Neuroaxial analgesia procedures Pregnancy

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

  • Istituto Giannina Gaslini

    Genova, GE, 16147, Italy

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