Clinical study to evaluate the effect of Panchasakara choorna in the management of Constipation.
Phase 3
Completed
- Conditions
- Health Condition 1: K590- Constipation
- Registration Number
- CTRI/2023/02/049981
- Lead Sponsor
- Rajiv Gandhi University of Health Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
Patient having symptoms of Vibandha (Constipation).
Patient who are fulfilling ROME IV Criteria for Constipation.
Patient who are fulfilling Bristol Stool Form Scale (1 to 2) for Constipation.
Only those patients willing to give the written informed consent.
Exclusion Criteria
Patients on chronic laxative medication.
Patients on medicines which are intended to cause constipation (like Calcium supplements, Iron supplements, Diuretics, Opioids, Analgesics, Antidepressant).
Patients suffering with hypertension.
Pregnant or lactating women.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in the frequency of bowel movement and changes in stool form with the administration of Panchasakara ChurnaTimepoint: Follow up of patients will be taken on Day 0, Day 7 and Day 14 where the <br/ ><br>assessment of symptoms will be done. Later on, Day 21, a follow up for assessing the <br/ ><br>relapse of symptoms would be carried out.
- Secondary Outcome Measures
Name Time Method Changes in the frequency of bowel movement and changes in stool form as per Bristol stool scaleTimepoint: Outcome will be assessed on Day 0, Day 7, Day 14 and Day 21