Effect of intravenous dexmedetomidine on duration of spinal anaesthesia with hyperbaric bupivacaine in patients undergoing lower abdominal surgeries
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Duration of sensory block motor block and analgesia in spinal anaesthesia
研究概览
简要总结
This prospective double blinded randomized controlled study evaluates the effect of intravenous dexmedetomidine on the duration and quality of spinal anaesthesia with hyperbaric bupivacaine in patients undergoing lower abdominal surgeries. Sixty patients belonging to ASA I and II aged 18 to 60 years are randomly divided into two groups one receiving IV dexmedetomidine and the other normal saline before spinal block. The study compares sensory and motor block duration analgesia hemodynamic stability sedation and adverse effects between two groups. The aim is to determine whether IV dexmedetomidine safely enhances spinal block duration and improves patient comfort and recovery.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients admitted for Elective lower abdominal surgeries under spinal anaesthesia with ASA grades 1 and 2.
排除标准
- •Patient refusal Contraindications to regional anaesthesia Patients with hepatic and renal impairment Patients taking Beta blockers and steroids.
结局指标
主要结局
Duration of sensory block motor block and analgesia in spinal anaesthesia
时间窗: Intraoperative period and postoperative period until full recovery of sensory and motor function up to 4 hours post spinal anaesthesia
次要结局
- Hemodynamic parameters Level of sedation and Adverse effects in spinal anaesthesia(Intraoperative period and postoperative period until full recovery of sensory and motor function up to 4 hours post spinal anaesthesia)
研究者
VARSHINI R V
PSG Institute of Medical Sciences and Research