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临床试验/NCT05851768
NCT05851768招募中不适用

Analgesic Efficacy of Adding Dexmedetomidine VS Magnesium Sulphate as Adjuvants With Bupivacaine in Ultrasound-guided Erector Spinae Plane Block for Post Thoracotomy Pain

National Cancer Institute, Egypt2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年5月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60
试验地点
2
主要终点
Total postoperative morphine consumption

研究概览

简要总结

Postoperative pain management is considered an integral part of perioperative care in patients undergoing thoracotomy. In order to reduce these complications, multiple regional techniques have been developed for thoracotomy including Intercostal nerve block, Erectospinae plane block and serratus block. Multiple adjuvants have been used in regional analgesia including adrenaline,clonidine,magnesium sulphate,dexmedatomidine and opoids.

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 (Care Provider, Investigator)

盲法说明

Double blinded

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age from 18 to 65 years.
  • Male and female sexes.
  • ASA I-II.,III
  • Cancer patients undergoing thoracotomy incisions
  • Body mass index (BMI) from 18.5 to 30 kg/m2

排除标准

  • Patient refusal
  • Known allergy to any of the used drugs
  • Low platelet count, any coagulation defect

研究组 & 干预措施

Erector spinae plane block with 0.25% bupivacaine

Active Comparator

Patients will receive ultrasound guided ESPB with 0.25% bupivacaine

干预措施: Bupivacaine (Drug)

Erector spinae plane block with 0.25% bupivacaine and Magnesium

Experimental

Patients will receive ultrasound guided ESPB with 0.25% bupivacaine and magnesium

干预措施: Bupivacaine + Magnesium (Drug)

Erector spinae plane block with 0.25% bupivacaine and Dexmedetomidine

Experimental

Patients will receive ultrasound guided ESPB with 0.25% bupivacaine and dexmedetomidine

干预措施: Bupivacaine + Dexmedetomidine (Drug)

结局指标

主要结局

Total postoperative morphine consumption

时间窗: First 24 hours postoperatively

Total dose of morphine needed postoperatively in the first 24 h

次要结局

  • Time to first postoperative rescue analgesia.(First 24 hours postoperatively)

研究者

发起方
National Cancer Institute, Egypt
申办方类型
Other
责任方
Principal Investigator
主要研究者

Walaa Youssef Elsabeeny

Assistant professor of Anesthesia and Pain management

National Cancer Institute, Egypt

研究点 (2)

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