跳至主要内容
临床试验/CTRI/2013/08/003937
CTRI/2013/08/003937尚未招募4 期

Study of the effect of intrathecal dexmedetomidine as an adjuvant in spinal anesthesia for Gynaecological Surgery.

Peoples Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2013年8月9日最近更新:

试验速览

阶段
4 期
状态
尚未招募
入组人数
60
试验地点
1
主要终点
motor block regession in bromage score,sensory

研究概览

简要总结

•Study the effect of intrathecal dexmedetomidine for prolongation of spinal analgesia..

OBJECTIVES:-

•To see the effect of intrathecal dexmedetomidine for prolongation of spinal analgesia.

•To study onset and level of sensory and motor block.

•To monitor the quality of analgesia with its duration.

•To study the side effects if any.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Outcome Assessor Blinded

入排标准

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

入选标准

  • 1.ASA grade I and II patients.
  • 2.Age group 18-60 years.
  • Gynecological surgeries.

排除标准

  • Patient refusal or unco-opretive patient
  • Bleeding disorder
  • Neurological deficit.
  • History of seizures 5.

结局指标

主要结局

motor block regession in bromage score,sensory

时间窗: 4 to 8 hours after intra thecal injection

block regession by pin prick senstion to

时间窗: 4 to 8 hours after intra thecal injection

analgesic in post operative period,any other side

时间窗: 4 to 8 hours after intra thecal injection

dermatomes,time to requirement to first

时间窗: 4 to 8 hours after intra thecal injection

effects like nausea,headache,itching etc

时间窗: 4 to 8 hours after intra thecal injection

次要结局

  • sensory block regession by pin prick senstion to(dermatomes,time to requirement to first)

研究者

申办方类型
Private medical college

研究点 (1)

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