Comparing two pain management techniques after breast surgery
A Comparative Study of Erector Spinae Plane Block and Serratus Posterior Superior Intercostal Plane Block on Postoperative Opioid Consumption Following Breast and Axillary Dissection Surgery: A Randomized Controlled Trial
NA · Medipol University · NCT06833697
This study is testing two different pain relief methods after breast surgery to see which one helps patients feel better while using fewer opioids.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Medipol University (other) |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06833697 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of two ultrasound-guided nerve blocks, the erector spinae plane block (ESPB) and the serratus posterior superior intercostal plane block (SPSIP), in reducing postoperative opioid consumption following breast surgery. It aims to determine which technique provides better pain relief while minimizing opioid-related side effects such as nausea and respiratory depression. The study will be conducted as a prospective, randomized controlled trial at Medipol Mega University Hospital, involving patients aged 18-80 scheduled for breast surgery with axillary lymph node dissection.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-80 who are scheduled for breast surgery with axillary lymph node dissection and classified as ASA physical status I-III.
Not a fit: Patients with a history of allergies to local anesthetics, pregnant women, or those with psychiatric or neurological disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies that reduce opioid use and enhance recovery for patients undergoing breast surgery.
How similar studies have performed: While both nerve blocks have been used effectively for pain management, this study is novel in directly comparing their efficacy in reducing opioid consumption after breast surgery.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * aged 18-80 years * Classified as ASA (American Society of Anesthesiologists) physical status I-III * Scheduled for breast surgery with axillary lymph node dissection Exclusion Criteria: * Patients with a history of allergies * allergic to local anesthetics * pregnant women * psychiatric or neurological disorders
Where this trial is running
Istanbul
- Medipol University — Istanbul, Turkey (RECRUITING)
Study contacts
- Study coordinator: Burak Ömür
- Email: bomur@medipol.edu.tr
- Phone: +905056215056
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Breast Surgery, Erector Spinae Plane Block, Serratus Posterior Superior Intercostal Plane Block, Breast surgery, Postoperative pain, Erector spinae plane block, Opioid consumption, Ultrasound-guided nerve block