跳至主要内容
临床试验/NCT05508451
NCT05508451已完成不适用

Comparison of the Efficacy of Tenoxicam, Paracetamol (Acetaminophen), and Tenoxicam-Paracetamol Combination on Postoperative Pain in Double-Jaw Surgery Patients

TC Erciyes University2 个研究点 分布在 2 个国家目标入组 80 人开始时间: 2018年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
80
试验地点
2
主要终点
The effects of tenoxicam, paracetamol, and tenoxicam-paracetamol combination on the postoperative 30th minute, first hour and 2th hour VAS (Visual Analog Scale) of double-jaw surgery patients.

研究概览

简要总结

Postoperative pain is generally caused by inflammation and oedema related to tissue trauma. Surgical tissue trauma is caused by many factors such as cotery-related burns, surgical incisions, dissections, and instrumental procedures like cutting, stretching, or compression.

The pain stimulus is triggered by mediators released by the traumatic tissue and transmitted to the spinal cord and then to the upper centres of the brain. Tenoxicam is an analgesic, anti-inflammatory, and antipyretic drug with a long duration of action, included in the oxicam subgroup of NSAIDs. Tenoxicam has been studied and found effective for many rheumatic diseases such as rheumatoid arthritis, ankylosing spondylitis, gout, extra-articular disorders, bursitis, tendonitis, and osteoarthritis. The primary aim of this study was to compare the effects of tenoxicam, paracetamol, and tenoxicam-paracetamol combination analgesic applications on the postoperative VAS score of double-jaw surgery patients. The secondary aim was to investigate the effects of these interventions on the number of both opioid and rescue analgesic drug consumption postoperatively.

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
Single (Investigator)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients between 18-50 aged of both genders who were scheduled for elective bimaxillary surgery
  • Classified as American Society of Anesthesiologists (ASA) risk class I or II

排除标准

  • having liver or renal dysfunction
  • coagulopathy disorder,
  • having psychiatric or medical conditions that might impair communication or compliance with the study procedures
  • having allergy or contra-indications to the study drugs .pregnancy.
  • patients who were planned to undergo additional simultaneous surgical procedures such as genioplasty were not included in the study. -

结局指标

主要结局

The effects of tenoxicam, paracetamol, and tenoxicam-paracetamol combination on the postoperative 30th minute, first hour and 2th hour VAS (Visual Analog Scale) of double-jaw surgery patients.

时间窗: at the first hour

VAS ( Pain intensity was assessed on a 100-mm Visual Analog Scale (VAS), where 0 = no pain and 100 = worst possible pain

The effects of tenoxicam, paracetamol, and tenoxicam-paracetamol combination

时间窗: at the 24th hour

VAS ( Pain intensity was assessed on a 100-mm Visual Analog Scale (VAS), where 0 = no pain and 100 = worst possible pain

次要结局

  • The secondary efficacy variable was the number of opioid and rescue drug consumptions during the postoperative 24 hours.(during the postoperative 24 hours.)

研究者

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

seher orbay yasli

Medical Doctor, Anesthesiologist

TC Erciyes University

研究点 (2)

Loading locations...

相似试验

Comparison of the Effects of Tenoxicam and... | 临床试验