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临床试验/CTRI/2025/01/079440
CTRI/2025/01/079440尚未招募4 期

Comparative Evaluation Of Equipotent Doses of Hyperbaric Bupivacaine And Ropivacaine In Perianal Surgeries a prospective randomized parallel group double blind study

RNT Medical College1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年2月10日最近更新:
适应症
相关药物

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
Duration of sensory block

研究概览

简要总结

My clinical study is comparasion of anaesthetic effects of intra thecal hyperbaric bupivacaine with hyperbaric ropivacaine in perianal surgeries in terms of durations of sensory block

kindly consider it for CTRI registrations .

研究设计

研究类型
Interventional
分配方式
Randomized
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

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

排除标准

  • •Patients refusal to participate in study, Patients having any absolute contraindications for saddle block eg coagulation abnormalities, platelet count less then 70,000, INR greater then 1.5, or on anticoagulants, Pregnant patient, Patients having systemic illness (like severe hypovolemia, raised intracranial pressure, neuromuscular diseases, ischemic/ valvular/ congenital heart diseases, psychiatric, hematological disorder).Any allergy to local anaesthetic, Short stature (height less then 150cm)with spinal deformity.

结局指标

主要结局

Duration of sensory block

时间窗: Postoperative 6 hours

次要结局

  • To study durations analgesia(To study duration of motor block)

研究者

申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Hemraj Tungaria

RNT medical College

研究点 (1)

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