跳至主要内容
临床试验/EUCTR2014-002215-42-IT
EUCTR2014-002215-42-IT进行中(未招募)1 期

Single-blind randomized controlled trial for acute abdomen analgesia in Pediatric Emergency department - Analgesia in acute pediatric abdominal pain

IRCCS Burlo Garofolo0 个研究点目标入组 300 人开始时间: 2014年7月3日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Children aged 4 to 18 years with acute abdominal pain defined as moderate severe (6-10 VAS or NRS scale)
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 300
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Assumption of acetaminophen 6 hours or NSAIDs or tramadol 8 hours before entering in the study
  • - protracted diarrhea with weight loss > 5%, refusal to eat or drink, drop in urine output
  • - known liver disease or kidney disease
  • - chronic neurological or metabolic action,
  • - positive history of bleeding or thrombocytopenia
  • - evidence of constipation and execution of barium evacuative

研究者

发起方
IRCCS Burlo Garofolo

相似试验