CTRI/2023/10/059111尚未招募Phase 3 4
A Comparative study to evaluate the efficacy of 0.75% Ropivacaine alone or combined with dexmedetomidine in supraclavicular brachial plexus block in upper limb surgeries.
试验速览
- 阶段
- Phase 3 4
- 状态
- 尚未招募
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- To determine whether the efficacy of 0.75% Ropivacaine with
研究概览
简要总结
it is a study to compare analgesic efficacy and motor blockade of 0.75% ropivacaine used alone or in combination with dexmedetomidine in upper limb surgeries.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Double Blind Double Dummy
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •120 patients of either sex, aged 18—60 years, belonging to American Society of Anesthesiologists (ASA) physical status class I and Il presenting for upper limb elective surgery under supraclavicular block.
排除标准
- •Who refuse to give consent.
- •With severe cardiac, renal, endocrine, pulmonary disease.
- •In physical status ASA grade Ill or higher.
- •Who are allergic to trial drugs.
- •Who are having local site infection.
- •With hemi-diaphragmatic paralysis on opposite side of surgery With any psychological disorder who would interfere with assessment of pain.
- •With history of brachial plexus injury.
- •With bilateral upper limb surgery and fracture.
- •With heart rate already on the lower side i.e 55 or less than 55b/m.
结局指标
主要结局
To determine whether the efficacy of 0.75% Ropivacaine with
时间窗: Onset & duration of Sensory block. Onset and duration of motor block. Duration of analgesia.
dexmedetomidine is greater than 0.75% Ropivacaine used alone in supraclavicular brachial plexus block for upper limb surgeries.
时间窗: Onset & duration of Sensory block. Onset and duration of motor block. Duration of analgesia.
次要结局
- To compare the Hemodynamic parameters Complications.
研究者
研究点 (1)
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