跳至主要内容
临床试验/CTRI/2021/11/037784
CTRI/2021/11/037784已完成不适用

COMPARATIVE STUDY OF DURATION OF ANALGESIA OFTRAMADOL VERSUS NALBUPHINE ADDED TO INTRATHECALBUPIVACAINE IN SPINAL ANAESTHESIA FOR INFRAUMBILICALSURGERIES.

Sree Balaji Medical College Hospital1 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2021年6月11日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
62
试验地点
1
主要终点
Duration of analgesia

研究概览

简要总结

This study was taken up to compare the commonly used opioids namely Tramadol and Nalbuphine as an adjuvant to spinal bupivacaine. Although these two drugs are safe and commonly used, only a few studies compared these two drugs.

We observed that nalbuphine was better than tramadol.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • 1.All elective infraumblical surgeries 2.ASA grade.

排除标准

  • 1.Patient refusal.
  • 2.ASA grade – III OR Above 3.Patients with complications like severe anaemia, hypovolemia, septicaemia, shock, spinal column abnormalities, previous spine surgery.
  • 4.Any contraindication to regional anaesthesia and with a known history of allergy to local anaesthetics / radioâ€opaque dye.
  • 5.Bleeding disorders or on anticoagulant therapy, Congenital or acquired coagulation disorders.
  • 6.Pregnancy.

结局指标

主要结局

Duration of analgesia

时间窗: Intrathecal administration of drugs is considered as baseline. From that time, this will be assesses every hourly until the first request of analgesia

次要结局

  • 1. Duration of sensory block(2. Duration of motor block)

研究者

申办方类型
Private medical college

研究点 (1)

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Comparison of two opioids in spinal anesthesia. | 临床试验