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Efficacy of a drug named probiotics in treating acute diarrhoea in adults

Not Applicable
Conditions
Health Condition 1: null- acute diarrhoea
Registration Number
CTRI/2018/04/013360
Lead Sponsor
Dr Meera Baby John
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

patients above 14years who have acute diarrhea

Exclusion Criteria

acute diarrhea who also have a serious complication ( renal failure , metabolic acidosis , severe dehydration , hypovolemic shock , heart failure)

History of allergy to lactobacillus spp.

H/o diarrhoea caused by amoeba (as evidenced by demonstration of motile trophozoites with blood in stool)colorectal cancer (as diagnosed by a per rectal examinationand/or endoscopic procedures where necessary).

Known allergy to study drugs

Patients who are already on probiotics

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine the efficacy of lactobacillus sporogenes in reducing the duration of diarrhoea in adults compared to placebo and it will be assessed for 7 daysTimepoint: To determine the efficacy of lactobacillus sporogenes in reducing the duration of diarrhoea in adults compared to placebo and it will be assessed for 7 days
Secondary Outcome Measures
NameTimeMethod
To establish the efficacy of lactobacillus sporogenes in reducing the frequency of loose stools,abdominal pain and hospital stay compared to placebo in adults with diarrhoeaTimepoint: 2 years
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