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C-Section pain showdown: nerve block vs. spinal morphine

NCT ID NCT06612424

Symptom relief Sponsor: Gaziosmanpasa Research and Education Hospital 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compared two methods for controlling pain after a planned C-section: a nerve block (quadratus lumborum block) and a spinal injection of morphine. 118 women who had a C-section under spinal anesthesia took part. The main goal was to see which method reduced the need for extra pain medicine in the first 24 hours after surgery.

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

118 people

The number who actually took part.

Started

Sep 2024

Finished

Apr 2025

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.

Ages

18 to 45 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: Inclusion Criteria: * Participants aged between 18 and 40 * ASA 2 risk group * Participants at 37-41 weeks of pregnancy * undergoing cesarean section under spinal anesthesia Exclusion Criteria: * The participant does not accept the procedure. * Patients with a history of eclampsia and preeclampsia during pregnancy * local anesthetic allergy * Infection at the procedure site * Anticoagulant use with bleeding disorder * Chronic analgesia and opioid use * Mental, psychiatric and neurological problems -Participant with ASA 3 and above with a history of any chronic disease. -

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

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

Postoperative pain

Contacts and locations

Locations

  • Gaziosmanpasa Research and Education Hospital, Istanbul, 34000

    Istanbul, 34255, Turkey (Türkiye)

More trials for these conditions

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