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临床试验/CTRI/2023/09/057665
CTRI/2023/09/057665尚未招募4 期

Comparative Evaluation Of Anaesthetic Effects Of Intra Thecal Hyperbaric Ropivacaine 0.75% With Or Without Fentanyl In Perianal Surgery: A Randomized Double-Blind Study

RNT Medical college1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2023年9月25日最近更新:

试验速览

阶段
4 期
状态
尚未招募
入组人数
66
试验地点
1
主要终点
Duration of analgesia

研究概览

简要总结

My clinical study is  Comparasion of  anaesthetic effects of   intra thecal hyperbaric ropivacaine 0.75% with or without fentanyl in perianal surgery****in terms of duration of analgesia block characteristic and side effect kindly consider it for CTRI registration.

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 60.00 Year(s)(—)
性别
All

入选标准

  • Patients with ASA physical status Grade I and II Posted for perianal surgeries under saddle block.

排除标准

  • Pregnant patients.
  • Patients having coagulation abnormalities, platelet count <70,000, INR >1.5, or on anticoagulants.
  • Patients having systemic illness (like severe hypovolemia, raised intracranial pressure, neuromuscular diseases, ischemic/ valvular/ congenital heart diseases, psychiatric, hematological disorder).
  • Patients having any absolute contraindications for spinal anaesthesia.
  • Patient refusal to participate in study.

结局指标

主要结局

Duration of analgesia

时间窗: Up to 6 hour post operatively

次要结局

  • To study block characteristics.(To study hemodynamic variables.)

研究者

申办方类型
Government medical college

研究点 (1)

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