Comparing nerve blocks for pain management in breast surgery
Official title: Comparison Between Ultrasound-guided Pectoral Nerve Blocks, Thoracic Erector Spinae Plane Block and Serratus Anterior Plane Block for Breast Surgery: A Prospective Randomized Study
Run by Tanta University · NCT06947642 · Data updated 2026-11-12
This study is testing which of three different nerve blocks can help women aged 21 to 65 manage pain better after breast surgery.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 21 Years to 65 Years |
| Sex | Women only |
| Enrollment | 60 (estimated) |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta, El-Gharbia) |
| Status | Recruiting |
| Started | April 30, 2025 |
| Main results expected | September 30, 2026 |
| Study ends | September 30, 2026 |
| Registry record updated | May 20, 2025 |
| Trial ID | NCT06947642 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are females aged 21 to 65 years old, classified as ASA physical status I or II, who are scheduled for elective breast surgeries under general anesthesia.
✕Probably not a fit
Patients who may not benefit from this study include those with a BMI of 35 kg/m2 or higher, those with coagulation abnormalities, or those with psychiatric disorders that affect communication.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to compare the effectiveness of three ultrasound-guided regional anesthetic techniques—Pectoral nerve block, Erector Spinae Plane block, and Serratus Anterior Plane block—in managing postoperative pain for patients undergoing elective breast surgeries. The research focuses on improving pain control, as inadequate management can lead to chronic pain and reliance on opioids, which have undesirable side effects. By utilizing these fascial plane blocks, the study seeks to reduce surgical stress response and enhance recovery outcomes for patients. The study will involve female participants aged 21 to 65 who are classified as ASA physical status I or II.
Why it matters
Potential benefit: If successful, this study could significantly improve postoperative pain management for breast surgery patients, reducing reliance on opioids and enhancing recovery.
How similar studies have gone: Previous studies have shown the efficacy of similar fascial plane blocks in managing postoperative pain, indicating that this approach is supported by existing evidence.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: • Age from 21 to 65 years old female, American Society of Anesthesiologists (ASA) physical status I or II, who will undergo breast surgeries under general anesthesia. Exclusion Criteria: * Patient refusal to participate in research. * Body Mass Index (BMI) ≥35 kg/m2. * Sensitivity to the intervention drugs. * Coagulation abnormalities. * Psychiatric disorder and communication difficulties. * Chronic neurological disease. * Any skin infection at the needle puncture site. * Chest wall deformity
Where it's running
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Tanta University
Tanta, El-Gharbia, Egypt Recruiting
Study contacts
- Study coordinator: Rehab S Taha, Master
- Email: rehabsalah2017@gmail.com
- Phone: 00201000507975
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.