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New study aims to reduce opioid use after breast surgery

NCT ID NCT07368413

Symptom relief Sponsor: Kayseri City 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 22, 2026 · Updated 2 times

Summary

This study compares two types of nerve blocks to manage pain and reduce opioid use in 70 adults having breast-conserving surgery. Participants will receive one of two ultrasound-guided injections before surgery. The goal is to see which method provides better pain relief and lowers the need for strong painkillers.

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

70 people

The number who actually took part.

Started

Apr 2026

Finished

Jul 2026

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 75 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: * Age between 18 and 75 years * ASA physical status I-III * No history of bleeding or coagulation disorders * Absence of neuropathy * Preoperative breast region NRS score \< 4 Exclusion Criteria: * systemic or regional infection * known allergy to local anesthetics * Unwillingness to participate in the study

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Conditions

The condition(s) this trial relates to.

breast cancer Pain

As listed by the trial registrant

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

Pain after surgery Pain management in breast surgery Regional anaesthesia

Contacts and locations

Locations

  • Kasyeri City Hospital

    Kayseri, Kocasinan, 38080, Turkey (Türkiye)

More trials for these conditions

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