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Which pain block works best after gynecologic cancer surgery?

NCT ID NCT06424938

Symptom relief Sponsor: Duygu Akyol 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This study compared two pain-blocking techniques—epidural block and erector spinae plane block—in 71 patients undergoing open gynecologic cancer surgery. Researchers measured pain scores, opioid use, and how quickly patients could move after surgery. The goal is to find which method provides better pain relief and faster recovery.

What this could mean

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

Active substance
epidural block or erector spinae plane block
What this could lead to
If one method works better, it could improve pain control and reduce opioid use after gynecologic cancer surgery.
What could go wrong
This is a small, completed study with 71 patients. Results may not apply to everyone, and neither method may be clearly better.

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

71 people

The number who actually took part.

Started

Jul 2024

Finished

Jan 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

30 to 70 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: * Patients who will undergo open abdominal surgery * Patients with ASAII-III * Those between the ages of 30-70 * Patients who are fully oriented and able to cooperate Exclusion Criteria: * Patients with ASAIV-V * Presence of active infection in the area where the block will be applied * Patients younger than 30 years old * Patients with BMI \> 40 * Patients who are allergic to bupivacaine * Chronic analgesic use

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Conditions

The condition(s) this trial relates to.

agnosia female reproductive organ cancer pain agnosia

As listed by the trial registrant

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

Analgesia Analgesia, epidural ERAS

Contacts and locations

Locations

  • Basaksehir Cam and Sakura City Hospital

    Istanbul, Turkey (Türkiye)

More trials for these conditions

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