A RANDOMISED CONTROLLED TRIAL TO COMPARE 0.75 PERCENTAGE HYPERBARIC ROPIVACAINE ALONE VERSUS 0.75 PERCENTAGE HYPERBARIC ROPIVACAINE WITH ADJUVANT FENTANYL FOR GYNECOLOGICAL SURGERIES UNDER SPINAL ANAESTHESIA
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- to observe time to onset and duration of sensory and motor blockade
研究概览
简要总结
we conducted a prospective randomised controlled trial of 100 patient of ASA grade 1 & 2 posted for elective gynecological surgeries under spinal anaesthesia. Group R receives 0.75% hyperbaic ropivacaine heavy 3 ml + 0.5 ml normal saline and Group RF receives 0.75% hyperbaric ropivacaine 3 ml + 25 mcg fentanyl. we compare the analgesic and anaesthetic efficacy in these two group.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 75.00 Year(s)（—）
- 性别
- Female
入选标准
- •elective gynecological surgeries informed and written consent.
排除标准
- •refusal of patients local site lumbar infection spine deformities coagulopathies major systemic illness.
结局指标
主要结局
to observe time to onset and duration of sensory and motor blockade
时间窗: after spinal anesthesia every 2 mins then every 5 min and every 19 min then every 30 mins and half hourly for 12 hours of spinal ananesthesia
NRS for post operative pain
时间窗: after spinal anesthesia every 2 mins then every 5 min and every 19 min then every 30 mins and half hourly for 12 hours of spinal ananesthesia
次要结局
- to observehemodynamics(perioperative)
研究者
Palak dineshbhai sitapara
GCS medical college, hospital and research centre