跳至主要内容
临床试验/NCT04618965
NCT04618965Unknown4 期

The Effect of Intrathecal Versus Intravenous Dexmeditomedine on Postoperative Analgesia in Transurethral Resection of the Prostate

Tanta University0 个研究点目标入组 75 人开始时间: 2020年11月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
75
主要终点
The time to first rescue analgesic

研究概览

简要总结

This study is to evaluate The analgesic effect of intrathecal versus intravenous dexmeditomedine in transurethral resection of the prostate

详细描述

This study will carried out in Tanta University hospital on75 male patients Patients will randomly classified into 3 groups Group I: will receive intrathecal hyperbaric bupivacaine 10mg in 2.5 ml and .5 ml saline with 3ml total volume Group II: will receive dexmeditomedine 5Mic diluted in.5 ml saline and hyperbaric bupivacaine 10mg in 2.5ml with 3ml total volume Group IIl: Will receive intravenous dexmeditomedine started at loading dose of 1 mic/kg diluted in 50 ml saline and administered within 10 min as loading dose , followed by maintenance at a dose of .4mic/kg/h diluted in200 ml saline till the end of surgery and hyperbaric bupivacaine 10 mg in 2.5 ml total volume

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
59 Years 至 70 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • male gender
  • 50:70years old

排除标准

  • contraindications of spinal anesthesia
  • Patient refusal
  • Patient taking alpha agonist or antagonist
  • Uncontrolled cardiac diseases
  • Allergy to local anesthetic drugs

研究组 & 干预措施

Control (Placebo) group

Placebo Comparator

Each patient will receive intrathecal hyperbaric bupivacaine 10 mg in 2.5 ml and 0.5 ml saline with 3 mL total volume. Continous 50 ml saline infusion for 10 min followed by 200 ml saline infusion till the end of surgery.

干预措施: control group (Drug)

Intrathecal dexmedetomidine group

Experimental

Each patient will receive dexmedetomidine 5 μg diluted in 0.5ml saline and hyperbaric Bupivacaine 10 mg in 2.5 ml with 3 mL total volume. Continous 50 ml saline infusion for 10 min followed by 200 ml saline infusion till the end of surgery.

干预措施: Intrathecal dexmedetomidine (Drug)

Intravenous dexmedetomidine group

Experimental

Each patient will receive intravenous dexmedetomidine started at a loading dose of 1 μg/kg diluted in 50 ml saline and administered within 10 min as a loading dose, followed by maintenance at a dose of 0.4 μg/kg/h diluted in 200 ml saline till the end of surgery and hyperbaric Bupivacaine 10 mg in 2.5 ml total volume.

干预措施: Intravenous dexmedetomidine (Drug)

结局指标

主要结局

The time to first rescue analgesic

时间窗: 24 hours postoperative

The duration between the administration of spinal block and the first desire for supplemental analgesia (onset of 1st post-operative analgesic dose). First post-operative analgesic dose will be1 μg/kg intravenous fentanyl when visual analogue pain score (VAS) is 4 or more

次要结局

  • Intraoperative and postoperative complications(Intraoperative and 24 hours postoperative)
  • Postoperative pain score Total dose of analgesic consumption I the first postoperative day Intraoperative and postoperative complications(24 hours postoperative)
  • Total analgesic consumption(24 hours postoperative)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Laila Elahwal

Lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine

Tanta University

相似试验