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临床试验/CTRI/2026/03/107046
CTRI/2026/03/107046尚未招募2 期

Comparative study of bupivacaine zero point five percent levobupivacaine zero point five percent and ropivacaine zero point seven five percent in spinal anaesthesia for daycare gynaecological procedures

Dr Jini S1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2026年4月12日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
75
试验地点
1
主要终点
To compare efficacy of zero point five percent hyperbaric bupivacaine zero point five percent hyperbaric levobupivacaine and zero point seven five percent hyperbaric ropivacaine for spinal anaesthesia in daycare gynaecological surgeries with respect to duration of sensory and motor block

研究概览

简要总结

THE USE OF SPINAL ANAESTHESIA IN GYNAECOLOGICAL SURGERIES HAS BEEN SHOWN TO PROVIDE EFFECTIVE AND COMFORTABLE INTRAOPERATIVE CONDITION THIS STUDY WILL HELP IN FINDING THE BEST OPTION FOR SPINAL ANAESTHESIA FOR DAYCARE GYNAECOLOGICAL SURGERIES WHICH WILL HELP IN FASTER RECOVERY AND EARLIER DISCHARGE WITH ADEQUATE SENSORY MOTOR BLOCK LESS TOXICITY AND STABLE HAEMODYNAMIC PARAMETERS

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator, Outcome Assessor and Date-entry Operator 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

  • •Asa status of one and two Height more than one forty five centimetres Written informed consent Posted for elective gynaecological surgeries.

排除标准

  • •History of bleeding diathesis and coagulopathy Patient refusal and coagulopathy History of allergy to local anaesthetics Spinal deformities or neurological disorders Infection at site of injection History of clinically relevant respiratory cardiac hepatic disorders.

结局指标

主要结局

To compare efficacy of zero point five percent hyperbaric bupivacaine zero point five percent hyperbaric levobupivacaine and zero point seven five percent hyperbaric ropivacaine for spinal anaesthesia in daycare gynaecological surgeries with respect to duration of sensory and motor block

时间窗: baseline immediately after injection two minutes five minutes ten minutess fifteen minutes twenty minutes thirty minutes sixty minutes ninety miutes one hundred and twenty minutes

次要结局

  • HAEMODYNAMIC CHANGES
  • SURGEON SATISFACTION
  • PATIENT SATISFACTION
  • SIDE EFFECTS IF ANY
  • Onset of sensory & motor block(baseline immediately after injection two minutes five minutes ten minutess fifteen minutes twenty minutes thirty minutes sixty minutes ninety miutes one hundred & twenty minutes)

研究者

发起方
Dr Jini S
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Jini S

Shimoga institute of medical sciences

研究点 (1)

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