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临床试验/CTRI/2024/03/064397
CTRI/2024/03/064397尚未招募4 期

A COMPARATIVE STUDY OF DEXMEDETOMIDINE DOSES (0.5MCG/KG VS 1MCG/KG) AS AN ADJUVANT TO 0.25% BUPIVACAINE FOR ULTRASOUND-GUIDED TRANSVERSUS ABDOMINIS PLANE (TAP) BLOCK IN CHILDREN UNDERGOING LAPAROSCOPIC SURGERIES

Army hospital R and R1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年3月29日最近更新:
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试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
50
试验地点
1
主要终点
To determine the difference of mean time to first rescue analgesia with 0.5mcg/kg and 1mcg/kg Dexmedetomidine in USG guided TAP Block for paediatric patients undergoing laparoscopic surgeries using CHEOPS pain scale
研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

Email has been accepted

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
2.00 Year(s) 至 10.00 Year(s)（—）
性别
All

入选标准

  • •Paediatric patients aged 2 to 10 years.
  • •(c) Patients with written informed consent of parents.

排除标准

  • •(a) Parental refusal to undergo the procedure.
  • •(b) Known allergy to the local anesthetic drug used in the procedure.
  • •(c) History of cardio vascular, respiratory disease and Hepatorenal insufficiency.
  • •(d) Presence of coagulopathies.
  • •(e) Patients taking Adrenoceptor agonist/ antagonist (f) Inability to comply with study requirements.

结局指标

主要结局

To determine the difference of mean time to first rescue analgesia with 0.5mcg/kg and 1mcg/kg Dexmedetomidine in USG guided TAP Block for paediatric patients undergoing laparoscopic surgeries using CHEOPS pain scale

时间窗: First 24 hours after surgery

次要结局

  • The total number of analgesic doses given in 24hrs after TAP Block in post op period(Upto 24hrs in post op period)

研究者

发起方
Army hospital R and R
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

SARANYA V

Army Hospital R and R

研究点 (1)

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