COMPARISON OF ANALGESIC EFFICACY OF BUTORPHANOL VERSUS DEXMEDITOMIDINE AS ADJUVANTS TO LEVOBUPIVACAINE IN ULTRASOUND GUIDED COSTOCLAVICULAR BLOCK: A PROSPECTIVE RANDOMIZED DOUBLE BLIND STUDY
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 46
- 试验地点
- 1
- 主要终点
- Duration of analgesia
研究概览
简要总结
This study is a e prospectivrandomized double blind study comparisionof analgesic efficacy of butorphanol versus dexmeditomidine as adjuvants to levobupivacaine in ultrasound guided costoclavicular blockthat will be conducted in sri sathya sai institute of higher medical sciences.
The primary outcome measures will be duration of analgesia who have received two different drugs for at 8months.
The secondary outcome will be
-
Onset of sensory blockade
-
Duration of sensory blockade
-
Onset of motor blockade
-
Duration of motor blockade
-
Hemodynamic variations in pulse rate, systolic blood pressure, diastolic blood pressure, spO2
-
Ramsay Sedation Score
-
Complications if any (nausea, vomiting, sedation, hypotension, bradycardia, respiratory depression)
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Not Applicable
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 who are willing to give consent to participate in the study.
- •Patients undergoing upper limb surgeries below elbow.
- •Patients between age : 18 to 60 years
- •ASA Grade I and Grade II patients.
排除标准
- •Patients with history of bleeding disorders.
- •Patients with local infection at the site of block.
- •Patients with epilepsy or other convulsive disorders.
- •Patients with documented neuromuscular disorders.
- •Patients with known allergy to local anaesthetic drugs.
结局指标
主要结局
Duration of analgesia
时间窗: Duration of analgesia was assessed using VAS score till 24 hrs postoperatively.
次要结局
- 1. Onset of sensory blockade(2. Duration of sensory blockade)