A clinical trial to study the effects of â??De-bloatâ?? capsules in female patients facing stomach discomfort and bloating.
Not Applicable
Completed
- Conditions
- Health Condition 1: K30- Functional dyspepsia
- Registration Number
- CTRI/2022/11/047380
- Lead Sponsor
- MOOM HEALTH PTE LTD
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 87
Inclusion Criteria
1 Female participants with Age between 25-40
years.
2 Females having regular menstrual cycle.
3 Subjects experiencing bloating after a heavy meal.
4 Females having bloating during their periods.
5 Willing to participate in the study after informed consent
Exclusion Criteria
Subject should not be on antacids, NSAIDs or herbal/ ayurvedic
medicine
2. Any subject who are taking any medication for bloating in the
preceding week.
3. Pregnant or lactating mother
4. Subject with life threatening cardiac, renal, pulmonary or
cardiovascular disease.
5. Severe disease requiring hospitalization /steroids /anti-cytokine
Therapy.
6. Subject taking antiplatelet drugs.
7. Subject with uncontrolled diabetes.
8. Subject with gall stone disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time to get relief from bloating symptoms such asborborygmus, <br/ ><br>eructation, early satiety, frequencies of defecation etc.This can <br/ ><br>also be relief from post food bloating or PMS bloating. <br/ ><br>Improvement in quality of lifeTimepoint: Visit 1 visit 2 visit3
- Secondary Outcome Measures
Name Time Method Improvement in quality of lifeTimepoint: Visit 1 visit 2 visit 3