CTRI/2022/09/045730尚未招募不适用
COMPARISON OF ROPIVACAINE WITH OR WITHOUT DEXMEDETOMIDINE IN ULTRASOUND GUIDED ERECTOR SPINAE PLANE BLOCK FOR POST OPERATIVE ANALGESIA AND ITS EFFECT ON RESPIRATOR FUNCTION IN PATIENTS UNDERGOING LAPAROSCOPIC CHOLECYSTECTOMY.
Dr S N MEDICAL COLLEGE2 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2022年9月22日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 66
- 试验地点
- 2
- 主要终点
- To compare quality of analgesia by Numerical Rating Scale (NRS) pain score and total opioid consumption during first 24 hours after LC.
研究概览
简要总结
The aim of our study is to compare the effect of dexmedetomidine as an adjuvant to local anaesthetic (Ropivacaine) combined with ESPB in postoperative pain relief in patients undergoing laparoscopic cholecystectomy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant and Investigator 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
- •The patients of age 18-65 yrs of either gender of ASA category I and II undergoing laparoscopic cholecystectomy surgery under general anaesthesia who are hemodynamically stable and declared fit in pre anaesthetic check-up.
排除标准
- •Patients of -ASA category III & IV, with significant neurological , psychiatric, neuromuscular, cardiovascular, pulmonary, renal or hepatic disease or having any anatomical abnormality, with history of any other biliary tract surgery, having any infections or pre existing wound at the site of injection, already a diagnosed case of chronic pain syndrome or on any prolonged opioid therapy, having any coagulopathy.
- •Patient’s refusal, or any history of lower abdominal surgery (adhesions).
- •Patients’ with history of any known or present psychiatric illness as the pain score cannot be assessed properly and with known neurological deficits.
- •Patients with history of allergy to the given medication.
- •Patients who are intubated and on mechanical ventilation, or with severe traumatic brain/spinal cord injury or in shock.
- •Surgeries who started as laparoscopic and then converted to open surgeries intra operatively or surgical time limit of laparoscopy exceeded 90minutes will be exempted from study.
结局指标
主要结局
To compare quality of analgesia by Numerical Rating Scale (NRS) pain score and total opioid consumption during first 24 hours after LC.
时间窗: To compare quality of analgesia by Numerical Rating Scale (NRS) pain score and total opioid consumption during first 24 hours after LC.
次要结局
- The following parameters will be compared between two groups:(a) Duration of analgesia (time for request of first rescue analgesia after surgery). b)Inspiratory Capacity (IC) preoperative and postoperative patients.)
研究者
研究点 (2)
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