跳至主要内容
临床试验/CTRI/2024/06/068995
CTRI/2024/06/068995尚未招募4 期

Effect of Erector spinae plane block on the Postoperative quality of recovery, using QoR-40 scale after laparoscopic Cholecystectomy- A randomized controlled clinical study

DR DN MEDICAL COLLEGE1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2024年6月26日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
66
试验地点
1
主要终点
to compare quality of recovery between group receiving Erector spinae plane block and control group during first 24 hours after Laparoscopic Cholecystectomy.

研究概览

简要总结

Laparoscopic abdominal surgeries are painful, even if they are minimal invasive, causing delayed recovery, increase opioid analgesic demand, increased hospital stay and cost. Hense giving pre-operative Erector Spinae Plane Block after intubation of patient under general anesthesia, patient can have stable intra operative hemodynamic parameters, good post operative pain relief and increase quality of recovery with less opioid analgesic need, early mobilization and reduced hospital stay and cost.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant 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

  • Patients of ASA grade 1 and 2 posted for elective laparoscopic cholecystectomy of duration less than 90 minutes.

排除标准

  • patients refusal to participate, known case of allergic to the study drug, having pre-existing wound at the site of injection, a case of chronic pain syndrome, on prolonged opioid therapy, coagulopathy, patient with history of previous abdominal surgeries, and surgery exceeding more than 90 minutes.

结局指标

主要结局

to compare quality of recovery between group receiving Erector spinae plane block and control group during first 24 hours after Laparoscopic Cholecystectomy.

时间窗: to compare quality of recovery between group receiving Erector spinae plane block and control group during first 24 hours after Laparoscopic Cholecystectomy.

次要结局

  • comparing between two groups The duration of Analgesia Cumulative dose of rescue analgesia & intra operative hemodynamic parameters.(Duration of analgesia is when the patient requires Painkiller & intra operative parameters are recorded at a defined interval. Outcome assessment will be started at Baseline & 5 min 10min 15min 20min 30min 40min 60min & 90min.)

研究者

发起方
DR DN MEDICAL COLLEGE
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Shobha Ujwal

DR. SN MEDICAL COLLEGE

研究点 (1)

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