IRCT2015010820610N1已完成未知
Evaluate the safety and efficacy of oral Tramadol in patients undergoing colonoscopy
Vice Chancellor for Research of Kermanshah University Of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 90
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20 years 至 65 years（—）
- 性别
- All
入选标准
- •Age between 20 to 65 years, for whatever reason are candidates for colonoscopy.
- •Exclusion criteria: People who have a history of drug abuse,People who have drug allergies, Heart disease, Or chronic systemic diseases.
排除标准
- 未提供
研究者
相似试验
尚未招募
3 期
Efficacy of orally administered Tramadol in reducing pain associated with hysteroscopic procedureCTRI/2016/10/007394JIPMER GOVERNMENT HOSPITA100
已完成
3 期
Comparison of efficacy and safety of Tramadol, Paroxetine and placebo in treatment of life long premature ejaculatioPremature ejaculation.Premature ejaculationIRCT201008304582N2rology Research Centre150
已完成
不适用
Safety and efficacy of tramadol in the treatment of refractory pain of interstitial cystitis: a double-blind, placebo-controlled, randomized prospective studyinterstitial cystitisJPRN-UMIN000009197Departmen of Urology, The University of Tokyo Hospital90
尚未招募
不适用
TRAMADOL VERSUS TAPENTADOL POSTOPERATIVE PAIN MANAGEMENTCTRI/2022/10/046753Dr MURUGANAND M
尚未招募
不适用
In-vivo Bioequivalence Test of Tramadol® tablet with brand drugs (ULTRAM® 100mg, Junssen Cilage, Switzerland).In this study, the disease is not examined. Subject bioequivalence test and reference tablets Tramadol studied..IRCT20200105046010N23Zagross Darou Pharmaceutical Company24