临床试验/NCT06658418

NCT06658418尚未招募1 期

Erector Spinae Plane Block with Dexmedetomidine and Bupivacain Versus Dexamethasone and Bupivacain for Postoperative Analgesia in Patients Undergoing Abdominal Surgeries

Loay Gamal0 个研究点目标入组 90 人开始时间: 2024年11月1日最近更新: 2024年10月26日

适应症

试验速览

阶段: 1 期
状态: 尚未招募
发起方
入组人数: 90
主要终点: VAS score

研究概览研究设计入排标准结局指标研究者记录与标识符相似试验

研究概览

简要总结

To compare the analgesic effect of dexmedetomidine combined with bupivacaine versus dexamethasone combined with bupivacaine for ultrasound-guided ESPB for postoperative pain control in patients scheduled for abdominal surgeries

研究设计

研究类型: Interventional
分配方式: Randomized
干预模型: Parallel
主要目的: Prevention
盲法: Double (Participant, Care Provider)

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: 否

入选标准

•Age :18 years old and older. Patients undergoing open abdominal surgery.

排除标准

•Patient refusal
•known sensitivity or contraindication to any of study drugs
•contraindications for local anesthesia
•Patients with local infection at site of puncture
•uncooperative patients
•history of psychological disorders or chronic pain and significant liver or renal disease.

结局指标

主要结局

VAS score

时间窗: at 30 minutes, 2, 4, 6, 8, 12, 16, 20, and 24 hours postoperative.

pain intensity using VAS score

次要结局

the time for requirement of first morphine dose(at 30 minutes, 2, 4, 6, 8, 12, 16, 20, and 24 hours postoperative.)

研究者

发起方

Loay Gamal

申办方类型

Other

责任方

Sponsor Investigator

主要研究者

Loay Gamal

LGamal

Assiut University

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