Health Condition 1: K590- Constipation
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Willing to provide written informed consent Diagnosed with functional constipation per Rome III criteria
Exclusion criteria
Exclusion criteria: Pregnant or lactating women Known hypersensitivity to investigational product components Use of other constipation treatments within the past 3 days Intestinal obstruction, severe gastritis, peptic/duodenal ulcer Patients deemed unfit by investigator s judgment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in frequency of bowel movements on 0th Day, 7th Day and 14th Day. Changes in stool consistency using the Bristol Stool Form Scale on 0th Day, 7th Day and 14th Day. Quality of Life (QoL) in terms of palatability, tolerability, and relief of constipation on 0th Day, 7th Day and 14th Day. Changes in CBC on 0th Day and 14th Day. Changes in Serum Electrolytes on 0th Day and 14th DayTimepoint: 0th Day, 7th Day and 14th Day. | — |
Secondary
| Measure | Time frame |
|---|---|
| NOT APPLICABLETimepoint: NOT APPLICABLE | — |
Countries
India
Contacts
KAHERs Shri B M Kankanawadi Ayurveda Mahavidyalaya