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Recruiting NCT07561853

NCT07561853 Serratus Posterior Superior vs Erector Spinae Plane Block for Breast Surgery

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Clinical Trial Summary
NCT ID NCT07561853
Status Recruiting
Phase —
Sponsor Sakarya University
Condition Postoperative Pain
Study Type INTERVENTIONAL
Enrollment 64 participants
Start Date 2026-06-01
Primary Completion 2026-11-15

Eligibility & Interventions

Sex All sexes
Min Age 25 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Serratus posterior superior intercostal plane blockErector Spinae Plane Block

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 64 participants in total. It began in 2026-06-01 with a primary completion date of 2026-11-15.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Postoperative pain after mastectomy remains a significant clinical problem that may impair patient comfort and delay early rehabilitation, potentially affecting functional recovery. Various analgesic techniques are used to manage postoperative pain. This study aims to compare serratus posterior superior intercostal plane block and erector spinae plane block, which are routinely used in our clinic for postoperative analgesia in patients undergoing mastectomy, in terms of ease of application and patient comfort.

Eligibility Criteria

Inclusion Criteria: * Female Gender * Mastectomy operation * 25-65 years * American Society Anestheosiology Physical Status I-III Exclusion Criteria: * American Society Anestheosiology Physical Status IV * Alcohol or substance abuse * Known allergy to local anesthetics or opioids * Severe psychiatric disorders

Frequently Asked Questions

Who can join the NCT07561853 clinical trial?

This trial is open to participants of all sexes, aged 25 Years or older, up to 65 Years, studying Postoperative Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07561853 currently recruiting?

Yes, NCT07561853 is actively recruiting participants. Visit ClinicalTrials.gov or contact Sakarya University to inquire about joining.

Where is the NCT07561853 trial being conducted?

This trial is being conducted at Sakarya, Turkey (Türkiye).

Who is sponsoring the NCT07561853 clinical trial?

NCT07561853 is sponsored by Sakarya University. The trial plans to enroll 64 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology