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临床试验/CTRI/2020/08/026995
CTRI/2020/08/026995尚未招募1 期

Comparison of analgesic efficacy of dexamethasone versus dexmedetomidine as an adjuvant to ropivacaine in ultrasound guided transverse abdominis block for postoperative pain relief in caesarean section

Dmch1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年5月8日最近更新:
适应症

试验速览

阶段
1 期
状态
尚未招募
发起方
Dmch
入组人数
100
试验地点
1
主要终点
Time to initial postoperative pain and first rescue analgesic.

研究概览

简要总结

Post operative caesarean patients have break through post op pain which will affects mother and baby. So we will give transverse abdominis peroneus block after completion of caesarean section with ropivacaine with dexmedetomidine or dexamethasone and compare the efficacy of dexmedetomidine versus dexamethasone as an adjunct to ropivacaine for post operative pain relief in caesarean section

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 45.00 Year(s)(—)
性别
Female

入选标准

  • 未提供

排除标准

  • •Any contraindication to spinal anesthesia; history of recent opioid exposure; hypersensitivity to any drugs used in study; significant cardiovascular, renal or hepatic diseases and known fetal abnormalities.

结局指标

主要结局

Time to initial postoperative pain and first rescue analgesic.

时间窗: outcome will be assessed immediately after shifting the patient to recovery, every hrly until the patient experience pain with VAS more than 3

Adverse effects if any

时间窗: outcome will be assessed immediately after shifting the patient to recovery, every hrly until the patient experience pain with VAS more than 3

次要结局

  • Time to initial rescue analgesic.(Adverse effects if any)

研究者

发起方
Dmch
申办方类型
Private medical college

研究点 (1)

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