跳至主要内容
临床试验/CTRI/2022/06/043314
CTRI/2022/06/043314尚未招募不适用

A study of assess the efficacy of ultrasound guided bilateral erector spinae block(ESPB) for abdominal surgery under general / spinal anaesthesia.

JLN MEDICAL COLLEGE AJMER1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2022年6月26日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
Comparison of Number and frequency of

研究概览

简要总结

Aim of our study is to assess the efficacy of erector spinae plane block (ESPB) for post operative analgesia in patients undergoing abdominal surgery under general / spinal  anaesthesia using Ropivacaine (0.25%) with dexmedetomidine  by creating a comparison with those without the block

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • •Age group between 18 and 60 years, Body weight 30 to 80kg , Patients belonging to ASA (American Society of Anaesthesiologists) class 1 and 2 Patients undergoing abdominal surgery of duration 1 to 2 hours in theatre with haemoglobin atleast 9 gm/dl, Patient free from any associated acute or chronic systemic illness.

排除标准

  • •Patients not willing to participate in the study Uncooperative patients Patient with chronic pain or on long-term analgesics Any known hypersensitivity or contraindication to bupivacaine Local pathology at the site of injection or disability limiting the performance of block,(deformity of spine) Patients receiving beta blockers or cardiac drugs.
  • •History of convulsion, allergy to the drug used, bleeding disorder, severe neurological deficit, thyroid disorder Patient with history of respiratory, cardiac, hepatic or renal disease (necessitating classification in ASA Class III or above) Patients having a history of significant neurological, psychiatric, or neuromuscular disorders Pregnant, lactating mothers.

结局指标

主要结局

Comparison of Number and frequency of

时间窗: Around 1 year

postoperative analgesia required in both the

时间窗: Around 1 year

groups for First 36 hours Postoperatively

时间窗: Around 1 year

To assess the effective analgesia by visual

时间窗: Around 1 year

analog scale (VAS) score

时间窗: Around 1 year

次要结局

  • to assess hemodynamic changes(to assess and compare the adverse effect)

研究者

发起方
JLN MEDICAL COLLEGE AJMER
申办方类型
Government medical college

研究点 (1)

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