Health Condition 1: K590- Constipation
Conditions
Interventions
None listed
Sponsors
Dr Viswanatham Ramakrishna
Eligibility
Inclusion criteria
Inclusion criteria: Male and Female participants whose age is more than 18 years and belown70 years Participants who are willing to give written signed informed consent to participate in the study Participants who are clinically diagnosed for constipation
Exclusion criteria
Exclusion criteria: Pregnant or breastfeeding or planning to become pregnant during the study period Known case of Hypersensitivity to Investigational drug content Patient using any other treatment for constipation in last 3 days Patients with signs of dehydration Known case of intestinal obstruction severe gastritis peptic or duodenal ulcer Patients who are not fit as per Investigator physician opinion
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Changes in Frequency of Loose stools from baseline and next day Changes in Bristol stool form scale from baseline and next day Timepoint: 0th, 1st day | — |
Primary
| Measure | Time frame |
|---|---|
| Relief from Constipation after single bed time oral administration Timepoint: 0th, 1st day | — |
Countries
India
Contacts
Public ContactDr Vedantam Giridhar
KAHERs Shri B M Kankanwadi Ayurved Mahavidyalaya
Outcome results
None listed