A study comparing New Nerve Block to Standard Pain Medicaltions in providing postoperative analgesia in patients undergoing breast surgeries

Authors
Category Primary study
Registry of TrialsClinical Trials Registry - India
Year 2026
INTERVENTION: Intervention1: Rhomboid Intercostal and Subserratus Plane Block: Ultrasound guided Rhomboid Intercostal and Subserratus Plane block with 30 mL of 0.25% bupivacaine This block has two components Rhomboid Intercostal Injection‐ T5 to T6 level Subserratus Plane Injection‐T6 to T8 level Control Intervention1: Standard Pain Medication: Intravenous Paracetamol 15mg/kg CONDITION: Health Condition 1: O‐ Medical and Surgical PRIMARY OUTCOME: Postoperative pain intensity assessed by NRS score at 2 hours after surgeryTimepoint: 2 hours after surgery SECONDARY OUTCOME: Postoperative NRS pain scores at rest and on movement at T0 0 min, 15 min, 1h, 2h, 4h, 6h, 12h, and 24h post‐surgery. ; ; Total opioid and rescue analgesic consumption over 24 hours postoperatively. ; ; Time to first rescue analgesia in minutes. ; ; Patient satisfaction score 0 to 10 scale. ; ; Incidence of Postoperative Nausea and Vomiting.Timepoint: Postoperative NRS pain scores at ; 0 minute ; 15 minutes ; 1 hour ; 2 hours ; 4 hours ; 6 hours ; 12 hours ; 24 hours INCLUSION CRITERIA: Elective unilateral breast surgery including Modified Radical Mastectomy, Breast Conservation Surgery, Simple Mastectomy, Fibroadenoma Female, 18 to 65 yrs, weight 40 to 80 kg American Society of Anaesthesiologist I,II
Epistemonikos ID: 83baf0cb37b4da59dd8b8b0e22c6096b9235d56d
First added on: Oct 08, 2026