跳至主要内容
临床试验/CTRI/2022/09/045730
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

发起方
Dr S N MEDICAL COLLEGE
申办方类型
Government medical college

研究点 (2)

Loading locations...

相似试验