CTRI/2025/09/095097尚未招募不适用
A prospective randomized double blind study to evaluate the effect of Dexamethasone 4 mg and Dexmedetomidine 1 microgram per kg as adjuvants to 0 point 2 percent Ropivacaine in bilateral superficial cervical plexus block for thyroid surgeries
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 105
- 试验地点
- 1
- 主要终点
- To assess duration of postoperative analgesia
研究概览
简要总结
The goal of our present study is to assess the analgesic efficacy of Ropivacaine (0.2%)
alone or with Dexmedetomidine (1µg/kg) or with Dexamethasone (4mg), in three groups
respectively in a double-blind fashion performed through bilateral superficial cervical plexus
block (BSCPB) after completion of surgery, with regard to duration of analgesia, pain intensity
scores (VAS), 24 hours postoperative tramadol requirements, and any complication after
thyroidectomy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 65.00 Year(s)（—）
- 性别
- All
入选标准
- •Elective thyroid surgeries under General Anaesthesia.
排除标准
- 未提供
结局指标
主要结局
To assess duration of postoperative analgesia
时间窗: AT BASELINE 0, 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 24 HOURS
次要结局
- I) To study the post-operative pain reduction, rescue analgesic requirement,(sedation in patients & patient satisfaction.)
研究者
Dr CHANDRASHEKAR M P
RNT MEDICAL COLLEGE
研究点 (1)
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