CTRI/2025/03/081759尚未招募2/3 期
A prospective randomised study comparing the efficacy of 0.25 % bupivacaine and 0.25% levobupivacaine in pectoral nerve type 2 block for postoperative pain relief in patients undergoing elective modified radical mastectomy
Department of anaesthesiology1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年3月27日最近更新:
试验速览
- 阶段
- 2/3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 70
- 试验地点
- 1
- 主要终点
- comparing the efficacy of 0.25% bupivacaine and 0.25% levobupivacaine in Carcinoma breast surgeries using PEC 2 block and the duration of postoperative analgesia
研究概览
简要总结
This study is a prospective randomised study comparing the efficacy of 0.25% bupivacaine and 0.25% levobupivacaine in PEC 2 block for postoperative pain relief in patients undergoing elective modified radical mastectomy surgery and to study the duration of postoperative analgesia
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 65.00 Year(s)（—）
- 性别
- Female
入选标准
- •All patients of ASA grade I and grade II patients between 18 to 65yrs.
排除标准
- •1]patient refusal to the procedure 2]any contraindications for regional anaesthesia technique like infection at the site of injection 3]coagulation disorder 4]drug allergy 5]history of other cancer 6]history of previous breast surgery 7]ASA grade IV 8]respiratory disease, cardiac disease and renal disease 9]having chemotherapy or radiotherapy in recent 8 weeks.
结局指标
主要结局
comparing the efficacy of 0.25% bupivacaine and 0.25% levobupivacaine in Carcinoma breast surgeries using PEC 2 block and the duration of postoperative analgesia
时间窗: 24 hours
次要结局
- total rescue analgesia required in the first 24hrs(24hrs)
研究者
Radhika G S
Mysore medical college and research institute
研究点 (1)
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