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Which painkiller helps moms recover fastest after C-Section?

NCT ID NCT06341049

Symptom relief Sponsor: Ataturk University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested three different ways to manage pain after a cesarean section (C-section) to see which helps mothers recover best. 120 women who had planned C-sections were randomly assigned to one of three pain relief methods. The researchers measured recovery using a simple questionnaire called ObsQoR-10 at 24 and 48 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

120 people

The number who actually took part.

Started

Mar 2024

Finished

May 2025

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 to 50 years

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: * Elective cesarean section under spinal anesthesia * Full-term singleton pregnancy * Agree to participate in the study * American Society of Anaesthesiology Score of II Exclusion Criteria: * Contrindication for neuraxial anesthesia * ASA≥3, diabetes, preeclampsia, cardiovascular disease, chronic pain and neuropathic pain * Age\< 18 or \> 50 * Multiple pregnancy * Presence of psychiatric diseases * Gave a history of allergic to any medication in the study protocol * Gave a history of chronic pain * Unable to consent * BMI\>35 kg/m2 * Those who were given opioids during the operation due to intraoperative pain * Those who have had previous abdominal surgery * Patients who failed spinal anesthesia and switched to general anesthesia * Those who have excessive bleeding or uterine atony during the operation * Does not understand VAS * Those who have a drain placed in the area to be infiltrated * Gave a history of drug addiction

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As listed by the trial registrant

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

Postoperative recovery

Contacts and locations

Locations

  • Ataturk University

    Erzurum, Palandoken, Turkey (Türkiye)

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