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Postoperative Analgesic Effectiveness of Fascial Plane Blocks in Breast Surgery

Recruitingn/aAges 18 Years - 80 YearsAllBursa Yuksek Ihtisas Training and Research Hospit…
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In plain words

What the trial is, and whether it could suit you

This prospective, single-center observational study will compare postoperative pain control in adults undergoing elective breast surgery. Ninety participants will be evaluated in three groups based on routine clinical care: rhomboid intercostal plane block, serratus posterior superior intercostal plane block, and control. The anesthesia method and fascial plane block will be selected by the treating anesthesiologist, and the research team will not assign participants to a group. The main outcome is the total amount of tramadol used through patient-controlled analgesia during the first 24 hours after surgery. Pain scores at rest and during movement, sensory block levels, postoperative nausea and vomiting, and block-related complications will also be recorded.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: * Age 18 to 80 years * American society of anesthesiologists physical status I to III * Undergoing surgery under general anesthesia * Provision of written informed consent * Scheduled for elective breast surgery Exclusion Criteria: * History of allergy to local anesthetic medications * Coagulation disorder * Body mass index greater than 40 kg/m2 * Infection at the block application site * Chronic pain syndrome * Pregnancy * Inability to communicate * Requirement for emergency surgery
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What it tests

  • Rhomboid intercostal plane block
  • Serratus posterior superior intercostal plane block
  • Control Group
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Where

1 site
Bursa Yuksek Ihtisas Training and Research Hospital
Bursa, Turkey (Türkiye)
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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