跳至主要内容
临床试验/CTRI/2025/08/093918
CTRI/2025/08/093918尚未招募不适用

Ultrasound guided continuous paravertebral versus thoracic epidural anaesthesia for postoperative pain relief in renal transplant recipients. A randomized controlled trial.

Dr Praveen Rijal1 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2025年9月8日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
68
试验地点
1
主要终点
To compare the analgesic effect (NRS) at rest of USG guided Paravertebral Block vs Thoracic Epidural Anaesthesia at six hour post surgery.

研究概览

简要总结

After selection of patients and randomization, patients will be divided into 2 groups, group A and group B. Group A will be USG guided continuous thoracic epidural anaesthesia and Group B will be USG guided continuous Paravertebral block using 0.125 percent bupivacaine 48 hours post surgery. They will be evaluated with total opiod consumption, dynamic NRS for pain.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • All patients undergoing kidney transplant surgery (living donor and cadaveric) aged 18-65years.

排除标准

  • Refusal of consent.
  • Patients with coagulation disorders.
  • Opioid addiction.
  • Allergy to local anaesthetics ( Bupivacaine).
  • Substance addiction or known psychiatric or mental problems.
  • Local infection of the skin where block is to be given.

结局指标

主要结局

To compare the analgesic effect (NRS) at rest of USG guided Paravertebral Block vs Thoracic Epidural Anaesthesia at six hour post surgery.

时间窗: Dynamic NRS at 6 hours post surgery.

次要结局

  • To compare total opioid(Tramadol) consumption.(During 48 hours post surgery)
  • Dynamic NRS on cough(at 0,2, 4 , 6 , 12, 24, 48-hour post surgery.)
  • To compare the complication such as post operative nausea & vomiting requiring rescue anti emetics , pruritis , hypotension , respiratory depression.(During 48 hours post surgery.)
  • To compare the procedure success rate, total procedure time, needle visibility, first-pass success rate, first-attempt success rate.(During 48 hours post surgery .)

研究者

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

Praveen Rijal

Post Graduated Institute of Medical Education and Research, Chandigarh

研究点 (1)

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