CTRI/2025/05/087076尚未招募4 期
Comparison of analgesic efficacy of Bupivacain and Ropivacain in Midpoint Transverse process to pleura block for Modified Radical Mastectomy
Pt JNM Medical College Raipur CG1 个研究点 分布在 1 个国家目标入组 128 人开始时间: 2025年5月20日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 128
- 试验地点
- 1
- 主要终点
- Post surgical analgesia using VAS score,as first rescue analgesic requirements.
研究概览
简要总结
This is a randomized Interventional study comparing two drugs I.e. inj. Ropivacaine 0.5% and inj. Bupivacaine 0.25% via midpoint transverse process to pleura block in patients undergoing modified radical mastectomy surgeries in terms of post surgical analgesic efficacy.
Patients will be enrolled with a sample size of 128 ( 64 in each group) , primary outcome will be first rescue analgesia duration using VAS score. Secondary outcome will be patient satisfaction using Likert score .
研究设计
- 研究类型
- Interventional
- 分配方式
- Random Number Table
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)(—)
- 性别
- Female
入选标准
- •ASA Grade 1 and 2 patients scheduled for elective MRM surgeries.
排除标准
- •Patient refusal Patient with COPD and lung disease Patient with severe liver disease Obesity with BMI more than 31 Patient on any analgesics Local site infections Local injury Allergic to study drugs.
结局指标
主要结局
Post surgical analgesia using VAS score,as first rescue analgesic requirements.
时间窗: Post surgical analgesia using VAS score at 0,2,4,8,10,12,16,20,24 and 48 hours, with Blood pressure, Heart rate, and SpO2 saturation
次要结局
- Patient satisfaction evaluated using, Likert scale(Liberty scale at 0,4,8,12,24 and 48 hours)
研究者
研究点 (1)
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