跳至主要内容
临床试验/NCT07531407
NCT07531407已完成不适用

The Effects of Dexamethasone and Ibuprofen on Postoperative Analgesia in Patients Undergoing Hand and Forearm Surgery With Axillary Brachial Plexus Block

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization1 个研究点 分布在 1 个国家目标入组 79 人开始时间: 2025年5月1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
已完成
发起方
入组人数
79
试验地点
1
主要终点
Duration of analgesia

研究概览

简要总结

This study aims to comparatively examine the effects of preemptive intravenous dexamethasone and intravenous ibuprofen use on the duration of analgesia in ultrasound-guided Axillary Brachial Plexus Block applications for patients undergoing hand and forearm surgery. Furthermore, investigating the relationship between the study drugs and the incidence of Postoperative Nausea and Vomiting and determining the time until the first use of rescue analgesic are also among the secondary objectives.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Patient's consent to participate in the study (Informed consent)
  • Aged between 18 and 65 years
  • ASA physical status I or II
  • Being oriented and cooperative
  • Scheduled to undergo hand or forearm surgery
  • Body Mass Index (BMI) below 40 kg/m²
  • Scheduled for axillary brachial plexus blockade

排除标准

  • Patient's refusal to participate in the study
  • Refusal of regional anesthesia
  • Known allergy to local anesthetics
  • Known allergy to ibuprofen
  • Known allergy to dexamethasone
  • Presence of coagulopathy
  • Local infection at the site of regional anesthesia application
  • Presence of malignancy at the surgical site
  • Diagnosis of diabetes mellitus
  • Body Mass Index (BMI) of 40 kg/m² or above
  • Duration of surgery exceeding 4 hours
  • Administration of opioid medication during the preoperative or intraoperative period

研究组 & 干预措施

D

Patients who had intravenouse dexamethasone

干预措施: IV Dexamethasone 8mg (Drug)

I

Patients who had intravenouse ibuprofen

干预措施: iv ibuprofen (Drug)

结局指标

主要结局

Duration of analgesia

时间窗: 24 hours

Duration of analgesia was defined as the time from the performance of the block until the patient's first report of pain.

次要结局

  • Incidence of PONV(24 hours)

研究者

发起方
Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ayşegül Bilen

Associate Professor

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

研究点 (1)

Loading locations...

相似试验