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Surgeon's simple trick slashes Post-Surgery pain

NCT ID NCT06905574

Symptom relief Sponsor: alperen can kokten 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 whether a nerve block given by the surgeon during breast reduction surgery could lower pain and the need for painkillers afterward. Sixty women took part, with half receiving the block. The goal was to see if this approach leads to less pain, less opioid use, and fewer side effects 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

60 people

The number who actually took part.

Started

Dec 2024

Finished

Oct 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 65 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: * Patient's willingness to be included in the study * 18-65 years * Woman * Operated with inferior pedicled breast reduction technique * The distance from the sternal notch to the nipple complex is between 25-40cm * ASA I-II * Breast Usg result BIRADS 1-2 * Patients who have not previously received RT to the breast and have no history of malignancy Exclusion Criteria: * Patient's request/refusal not to be included in the study * Previous history of malignancy * RT story, * ASA 3-4-5-patient group * Severe organ failure * Alcohol, drug addiction * Bupivacaine allergy * Diagnosis of psychiatric illness and psychiatric drug use * Surgery lasting longer than 3 hours * Bleeding diathesis

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As listed by the trial registrant

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

Breast reduction Postoperative pain control

Contacts and locations

Locations

  • Samsun training and research hospital

    Samsun, 55020, Turkey (Türkiye)

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