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临床试验/NCT03633344
NCT03633344已完成2 期

Efficacy of the Administration of Colloidal Silicon Dioxide in Tablet Dosage Form (Carbowhite) in Patients With Acute Diarrhea.

Omnifarma Kiev LLC0 个研究点目标入组 145 人开始时间: 2016年3月29日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
145
主要终点
Reduction in Frequency of Defecation to 3 Times Per Day

研究概览

简要总结

The purpose of the study is to demonstrate the antidiarrheal efficacy of colloidal silicon dioxide in tablet dosage form (Carbowhite) in patients with acute diarrhea.

详细描述

Background: Diarrhea is a medical condition characterized by frequent stool, more than 3 times (and more than 5-7 times in newborns) within the last 24 hours, and/or loose stool. The fecal matter is liquid, its daily mass exceeds 200 g per day, and water content reaches 95%.

Objectives: To demonstrate the antidiarrheal efficacy of colloidal silicon dioxide in tablet dosage form (Carbowhite) in patients with acute diarrhea.

Methods: A randomized clinical trial, double-blind, placebo-controlled, multi-center.

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, Investigator)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • signed Informed Consent Form for patient's study participation
  • male and female patients at the ages from 18 to 55 years
  • acute diarrhea (more than three episodes of liquid stool a day) within 48 hours or less in patients with usually normal stool
  • body temperature of ≤ 38 °C
  • patient's ability to adequately cooperate in the process of study

排除标准

  • aged of <18 or >55 years;
  • blood or pus in stool;
  • body temperature of >38 °C;
  • episodes of acute diarrhea for the last 30 days;
  • administration of antidiarrheal products for the last 24 hours;
  • salmonellosis (Salmonella of any serotype different from S. typhi and S. paratyphi; ICD-10: A02.0), dysentery (Shigella dysenteriae, Shigella flexneri, Shigella boydii; ICD-10: A03.0-A03.3), colibacillosis (Escherichia coli; ICD-10: A04.0-A04.4) which require administration of antimicrobial products;
  • pregnancy, lactation;
  • concomitant decompensated diseases or acute conditions which, according to an investigator, may affect study results
  • alcoholism and drug abuse;
  • participation in any other clinical study.

研究组 & 干预措施

Carbowhite

Active Comparator

3 tablets as a single dose (210 mg х 3 = 630 mg) TID (630 mg х 3 = 1,890 mg)

干预措施: Carbowhite (Drug)

Carbowhite placebo

Placebo Comparator

3 tablets as a single dose (210 mg х 3 = 630 mg) TID (630 mg х 3 = 1,890 mg)

干预措施: Carbowhite placebo (Drug)

结局指标

主要结局

Reduction in Frequency of Defecation to 3 Times Per Day

时间窗: From randomisation up to 5 days

Percent of patients administered the investigational production who achieved the efficacy endpoint (reduction in frequency of defecation to 3 times per day, absence of loose stool) on Day 5 or earlier

次要结局

  • Compliance Rate(From randomisation up to 5 days)
  • Duration of Treatment(From randomisation up to 5 days)
  • Quantity of Used Medication(From randomisation up to 5 days)

研究者

发起方
Omnifarma Kiev LLC
申办方类型
Industry
责任方
Sponsor

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