跳至主要内容
临床试验/NCT05705050
NCT05705050已完成不适用

Effect of Intraoperative Aminophylline Infusion on Pain Intensity After Ureterocopic Lithotripsy Surgeries

Tanta University1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2023年2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
已完成
入组人数
50
试验地点
1
主要终点
Intensity of pain

研究概览

简要总结

This study will be conducted to evaluate the effect of intraoperative systemic aminophylline infusion on pain intensity in patients undergoing ureteroscopic lithotripsy surgeries with ureteric stent placement at the end of the procedure.

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

入选标准

  • Aged between 18 to 50 years
  • American society of anesthesiology (ASA) physical status I - II
  • Body mass index (BMI) less than 30.0 kg/m2
  • Scheduled for ureteroscopic lithotripsy surgery with D-J ureteric stent placement at the end of procedure
  • Under general anesthesia.

排除标准

  • Patients with central nervous system diseases, cardiovascular diseases, arrhythmias, cerebrovascular diseases, convulsions, renal impairment or hepatic dysfunction.
  • Pregnancy or lactation.
  • Patients with a history of allergy to aminophylline.
  • Coffee consumption (more than 2 cups/day)
  • Patients with opioid addiction or patients treated with B agonists, tranquilizers, or antidepressants.
  • Short procedures less than 30 minutes or procedures not requiring D-J stent placement.

研究组 & 干预措施

Aminophylline group

Experimental

Patients will receive 4 mg/kg aminophylline diluted in 100 ml normal saline over 20 minutes after induction of anesthesia and positioning of patients in lithotomy position.

干预措施: Aminophylline group (Drug)

Control group

Placebo Comparator

Patients will receive 100 ml normal saline over 20 minutes after induction and lithotomy positioning.

干预措施: Control group (Other)

结局指标

主要结局

Intensity of pain

时间窗: In post anesthesia care unit (PACU)

Visual analogue score (VAS) score: will be measured on arrival to PACU, at 30 minutes, 1 hour, 2 hour, 6, 12 and 24 hour after surgery.

次要结局

  • The incidence of postoperative adverse reactions(24 hour after surgery)
  • Intensity of pain(24 hour after surgery)
  • Total amount of opioid dose(24 hour after surgery)

研究者

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

Osama Rehab

Lecturer of Anesthesiology, Intensive Care and Pain Medicine

Tanta University

研究点 (1)

Loading locations...

相似试验

Aminophylline Infusion on Pain Intensity After... | 临床试验