CTRI/2017/05/008449已完成4 期
Efficacy and safety of fixed dose combination of drotaverine hydrochloride(80 mg)and paracetamol(500 mg) in amelioration of abdominal pain in acute infectious gastroenteritis: a double blind randomized controlled trial
Walter Bushnell Pvt Ltd0 个研究点目标入组 250 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 250
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
入选标准
- •1.Patients between 18 to 59 years of either gender with presenting with acute infectious diarrhoea (defined as at least 3 unformed, watery or soft, stools accompanied by symptoms within 24 hours preceding randomization with duration of illness <= 72 hours) who present with moderate to severe (baseline pain intensity [PI] score on a 100-mm visual analog scale [VAS] of > 50 mm and â??moderate to severeâ?? on a VRS scale) abdominal pain present at enrollment.
- •2.Patients who give written informed consent with videography prior to the study entry.
- •3.Patients with good health as determined by:
- •Medical history
- •Physical examination
- •Clinical judgment of the investigator
排除标准
- •1.Patients with moderate or severe dehydration requiring hospitalization and administration of intravenous medications.
- •2.Patients with bloody diarrhoea and dysentery.
- •3.Any previous clinical history of gastroduodenal ulcer, gastrointestinal bleeding, or gastroduodenal perforation.
- •4.Concomitant use of medications that are known to increase the likelihood of upper gastrointestinal adverse events (e.g. corticosteroids and anticoagulants).
- •5.Patients with other established etiologies as pancreatitis, inflammatory bowel disease (IBD) or irritable bowel disease (IBS), previous gastrointestinal surgery and known immunodeficiency.
- •6.Patients with history of hypersensitivity to paracetamol and/or drotaverine.
- •7.Patients taking opioid analgesics, NSAIDs, and sedatives in the last 24 hours.
- •8.Presence of serious co-morbidity, such as cardiovascular disease, cerebrovascular disease, renal or hepatic impairment, diabetes, hypertension, hypo or hyperthyroidism.
- •9.Pregnant & lactating women.
- •10.Patients participating in any other clinical trial.
研究者
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