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临床试验/TCTR20240515001
TCTR20240515001尚未招募2 期

Optimal dose of simethicone administration for enhancing visibility prior to upper endoscopy A randomized, double blinded, placebo multicenter controlled trial

Internal medicine department, Suratthani Hospital0 个研究点目标入组 273 人开始时间: 2024年5月15日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
273

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
18 Years 至 80 Years(—)
性别
All

入选标准

  • 1. Chronic dyspepsia, 2. Dysphagia, 3. Esophageal varices surveillance, 4. Anemia, 5. Weight loss, 6. Vomiting, 7. Gastroesophageal reflux disease symptoms

排除标准

  • 1. Upper GI bleeding, 2. Peritonitis, 3. Esophageal stricture or gastric outlet obstruction, 4. Active cardiac condition or respiratory failure, 5. Pregnancy or lactation, 6. Previous history of abdominal surgery, 7. Allergy to simethicone, 8. Not cooperate to perform an EGD

研究者

发起方
Internal medicine department, Suratthani Hospital

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