Clinical trial

A Randomized Single-Blind Controlled Trial Comparing the Efficacy of Nitazoxanide Versus Rifaximin in Adult Patients With Irritable Bowel Syndrome Without Constipation

Name
202207MH1
Description
This study aim to compare the efficacy of nitazoxanide in 2-week course of treatment with rifaximin in treating diarrhea associated with IBS. We also aim to study its effect over 10 weeks after treatment to evaluate its efficacy in eradicating symptoms of IBS in the long run.
Trial arms
Trial start
2022-07-01
Estimated PCD
2024-07-01
Trial end
2024-12-31
Status
Recruiting
Phase
Early phase I
Treatment
Nitazoxanide 500Mg Oral Tablet
patients receiving treatment with Nitazoxanide 500 mg two times daily for 14 days
Arms:
Nitazoxanide
Rifaximin 550Mg Tab
patients receiving treatment rifaximin at a dose of 550 mg three times daily for 14 days
Arms:
Rifaximin
Size
84
Primary endpoint
Proportion of Subjects Who Had Adequate Relief of Global IBS Symptoms for at Least 2 of the 4 Weeks During the Primary Evaluation Period
6 weeks
Eligibility criteria
Inclusion Criteria: * Patients 18 years of age or older. * Patients suffering from diarrhea-predominant IBS according to Rome III criteria. * Active symptoms for at least 2 weeks * Abdominal Pain Intensity: weekly average of worst daily (in past 24 hours) abdominal pain score of \> 3.0 on a 0-to-10-point scale and Stool Consistency: at least one stool with a consistency of Type 6 or Type 7 Bristol stool score (BSS) on at least 2 days per week * Report no restriction whatsoever on their diet. Exclusion Criteria: * Presence of liver disease, malignancy, severe malabsorption, bedridden, endocrinological disorders, or severe chronic obstructive pulmonary disease. * Patients who have undergone abdominal surgeries except for appendectomy and/or cholecystectomy and/or hysterectomy. * Patients who consumed any medications that may affect bowel function within the last 2 weeks such as antibiotics, probiotics, prebiotics, antispasmodics, antidiarrheals, narcotics, or any other medication that may alter bowel function * Patients on antidepressants or antipsychotics starting within the last six weeks before eligibility check.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1', 'PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['PARTICIPANT']}}, 'enrollmentInfo': {'count': 84, 'type': 'ESTIMATED'}}
Updated at
2023-11-21

1 organization

2 products

1 indication

Product
Rifaximin