跳至主要内容
临床试验/ACTRN12624000061538
ACTRN12624000061538尚未招募Unknown

RCT: a Comparison between a fixed intrathecal dose of 0.5% Hyperbaric Bupivacaine, and tailored intrathecal dose of 0.5% Hyperbaric Bupivacaine based on a modified Harten's Chart in non pregnant patients.

Ministry of Health0 个研究点目标入组 240 人开始时间: 2024年1月25日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
入组人数
240

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Blinded (masking used)

入排标准

年龄范围
20 Years 至 55 Years(—)
性别
All

入选标准

  • Patient age from 20 years of age to 55 years of age
  • Male and female
  • Surgical Procedures eligible for Spinal anesthesia.

排除标准

  • Patient Refusal
  • History of Spine Surgery.
  • Morbidly Obese
  • ASA IV or more
  • Central Nervous system disease
  • Patient diagnosed with a condition that may affect the Capacity and normal physiology or anatomy of the BBB or intrathecal space
  • hepatic dysfunction
  • Patient who require > 2 trials of Spinal Anesthesia.
  • Patient with contraindications to spinal anesthesia.
  • renal dysfunction
  • Failed Spinal anesthesia and the need to convert to General anesthesia
  • Surgeries that requires > 120 minutes
  • Chronic pain Syndrome.
  • Drug Addiction
  • Allergy to Local Anesthetics

研究者

相似试验