Clinical study to evaluate the effect of Panchasakara choorna in the management of Constipation.

A clinical study to evaluate the effect of Panchasakara Choorna in the management of Vibandha.

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/02/049981

Enrollment

Registered

2023-02-22

Start date

Unknown

Completion date

Unknown

Last updated

2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K590- Constipation

Interventions

None listed

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

Measure	Time frame
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 assessment of symptoms will be done. Later on, Day 21, a follow up for assessing the relapse of symptoms would be carried out.	—

Secondary

Measure	Time frame
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	—

Countries

India

Contacts

Public ContactShravana L

SDM Institute of Ayurveda and Hospital, Bengaluru

drsmithajain@sdmayurbanagalore.in9480063676

Outcome results