Effect of Aniseed in treatment of gastrointestinal symptoms in Coronavirus disease
Phase 3
- Conditions
- COVID-19 infection.Covid-19, confirmed cases, positive test resultU07.1
- Registration Number
- IRCT20120506009651N3
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 225
Inclusion Criteria
Patients from 18 years old to 70 years old with a diagnosis of Coronavirus based on clinical and laboratory symptoms; hospitalization, home quarantine and outpatients
Diarrhea, anorexia, nausea or vomiting and abdominal pain within 24-48 hr
Exclusion Criteria
Pregnant or nursing females
Organic disorders with survival time of less than 3 days
Significant allergic reactions to the herbal drug
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Diarrhea. Timepoint: Before and after intervention. Method of measurement: Visual analogue scale (VAS) questionnaire which graded from zero (no sign) to 10 (severe sign).;Anorexia. Timepoint: Before and after intervention. Method of measurement: Visual analogue scale (VAS) questionnaire which graded from zero (no sign) to 10 (severe sign).;Abdominal pain. Timepoint: Before and after intervention. Method of measurement: Visual analogue scale (VAS) questionnaire which graded from zero (no sign) to 10 (severe sign).
- Secondary Outcome Measures
Name Time Method Gastrointestinal disorders. Timepoint: End of Treatment (2 weeks after starting intervention). Method of measurement: Visual analogue scale (VAS) questionnaire.