跳至主要内容
临床试验/CTRI/2023/12/060570
CTRI/2023/12/060570尚未招募Unknown

A prospective study to access the efficacy of Clonidine and Fentanyl as adjuvants to Hyperbaric Ropivacaine in infra umbilical surgeries performed under spinal anaesthesia

Office of principal midnapore medical College and hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年1月15日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
Comparing block characteristics in respect to sensory block, motor block and duration of post operative analgesia

研究概览

简要总结

Comparison between intrathecal fentanyl and clonidine as adjuvants to hyperbaric ropivacaine in subarachnoid block for elective lower abdominal surgeries under spinal anaesthesia: A prospective, randomised, double blinded, comparative study.

To compare the duration of motor and sensory block of intrathecal 25mcg fentanyl and intrathecal 30mcg clonidine along with 0.75% hyperbaric ropivacaine.

To compare the post operative analgesia in patients given intrathecal fentanyl and intrathecal clonidine.

To compare the side effects and complications (if any) of the given drug during intraoperative and post operative period.

This is a hospital based, prospective, randomised, double blinded, comparative analytical study on cohort of patients posted for elective lower abdominal surgeries under subarachnoid block in general surgery operation theatre Midnapore Medical College and hospital.

As we are using equipotent dose of fentanyl and clonidine and both increases duration of block and postoperative analgesia we expect both the group receiving fentanyl and clonidine will have a longer duration of block and postoperative analgesia but among both the groups which one will provide longer duration of block and postoperative analgesia will be known after completion of the. study

研究设计

研究类型
Observational

入排标准

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

入选标准

  • Inclusion criteria: 1.ASA grade 1&2
  • Age group of 18-60 years
  • Body mass index between 18.5-24
  • Elective lower abdominal surgeries under spinal anaesthesia.

排除标准

  • Patients with severe cardio- respiratory disease
  • Patients with hepatic and renal disease
  • Patients with neurological disorders
  • Patients with endocrine disorders
  • Subarachnoid block failure
  • Any contraindications for spinal anaesthesia
  • Drug allergy to study drug.

结局指标

主要结局

Comparing block characteristics in respect to sensory block, motor block and duration of post operative analgesia

时间窗: before spinal, after spinal, at 5,10,15,20,25,30,40,50,60,70, 80,90 min after spinal or till completion of surgery and 2hr, 4hr, 10hr, 14hr,18hr, 22hrs, 24 hrs post op

次要结局

  • 1. Highest level of sensory block(2. quality of motor block)

研究者

发起方
Office of principal midnapore medical College and hospital
申办方类型
Government medical college

研究点 (1)

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