SPSIP Block Versus ESP Block for Chronic Pain After Unilateral Breast Surgery
Recruiting
N/A
Interventional Study
Postoperative Pain
Opioid Use
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 65
- Sex
- Female
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 90 (estimated)
- Sponsor
- Engin Çetin · Government
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About This Trial
This prospective, randomized, assessor-blinded study will compare serratus posterior superior intercostal plane block and erector spinae plane block in adult female patients undergoing unilateral breast surgery. The primary outcome is chronic postoperative pain at 3 months, assessed using the Brief Pain Inventory-Short Form.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Female patients aged 18-65 years
* ASA physical status I-III
* Body mass index (BMI) between 18 and 35 kg/m²
* Scheduled for elective unilateral breast surgery (mastectomy with or without sentinel lymph node biopsy)
* Ability to understand and provide written informed consent
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Contacts