NCT07257874已完成3 期
Comparison Between Intra-Operative Pectoral Block and Intravenous Analgesia for Post-Operative Pain Relief in Patients Undergoing Modified Radical Mastectomy
Islamabad Medical and Dental College2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年7月1日最近更新:
干预措施
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 2
- 主要终点
- Postoperative Pain Severity at 24 hours Measured by Numeric Pain Rating Scale from 0-10 , where 0 is no pain and 10 is severe pain.
研究概览
简要总结
There is difference in post operative pain between patients receiving inter- pectoral block and those receiving standard Intravenous analgesia(INJ TORADOL) in patients undergoing Modified Radical Mastectomy.
To compare between these two methods , which one is better for post operative pain management.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Female Patients undergoing Modified Radical Mastectomy for biopsy proven Carcinoma Breast
- •Patient with age 18-65 years
- •Patients with ASA Grade 2
- •BMI less than 40 kg/meter square
排除标准
- •Block site infection
- •Coagulopathies (INR > 1.6 and Platelets < 100000)
- •Any Organ dysfunction such as severe cardiac, pulmonary, renal or liver dysfunction
- •Systemic infection
- •Known hypersensitivity to local anesthetic agents
研究组 & 干预措施
PECs Arm
Experimental
干预措施: bupivacaine 0.5% injection (Drug)
IV Analgesia Arm
Active Comparator
干预措施: Ketorolac 30 mg IV (Drug)
结局指标
主要结局
Postoperative Pain Severity at 24 hours Measured by Numeric Pain Rating Scale from 0-10 , where 0 is no pain and 10 is severe pain.
时间窗: 24 hours Post Surgery
次要结局
未报告次要终点
研究者
研究点 (2)
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