CTRI/2025/04/085614尚未招募4 期
A comparative evaluation of scalp block using 0.5% bupivacaine with dexamethasone versus 0.5% bupivacaine alone for attenuating postoperative pain in patients undergoing supratentotial craniotomy under general anaesthesia
Sardar Patel medical college1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2025年5月2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
- 66
- 试验地点
- 1
- 主要终点
- To compare the efficacy and safety of bupivacaine and dexamethasone as adjuvant in scalp block for supratentorial craniotomy in terms of:
研究概览
简要总结
Our study aimed at comparing postoperative analgesia assessment using bupivacaine with dexamethasone and bupivacaine alone in scalp block for supratentorial craniotomy .
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Double
入排标准
- 年龄范围
- 18.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •Posted for elective supratentorial craniotomy BMI 18-30 Kg/m² ASA grade I-II.
排除标准
- •Patient refusal Known allergy to bupivacaine used in the study Patient with ASA grade III and above Glasgow Coma Score (GCS) less than 15 Hepatic, renal or cardiorespiratory failure Patients undergoing emergency procedure.
结局指标
主要结局
To compare the efficacy and safety of bupivacaine and dexamethasone as adjuvant in scalp block for supratentorial craniotomy in terms of:
时间窗: Evaluate on the basis of VAS score in first 24 hours postoperatively
Duration of postoperative analgesia.
时间窗: Evaluate on the basis of VAS score in first 24 hours postoperatively
Requirement of first rescue analgesia and total number of rescue analgesics
时间窗: Evaluate on the basis of VAS score in first 24 hours postoperatively
次要结局
- To observe(Postoperative hemodynamic parameters)
研究者
Siddhi Tiwari
Sardar Patel Medical College, Bikaner, Rajasthan
研究点 (1)
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