Skip to content

Study of large intestine in retention of faeces in relation with fecal calprotectin

Study of pakvashaya pertaining to purishaja udavarta with reference to investigation range of fecal calprotectin

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/12/048079
Enrollment
120
Registered
2022-12-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: K638- Other specified diseases of intestine

Interventions

None listed

Sponsors

Dr Sachin Rangrao Patil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Selected 120 diagnosed patients of purishaja udavarta

Exclusion criteria

Exclusion criteria: Patients below 40 years and above 60 years Avirecya Patients taken non-steroidal anti-inflammatory drugs.

Design outcomes

Primary

MeasureTime frame
Assessment of pakvashaya is possible on the basis of investigation range of fecal calprotectinTimepoint: 3 weeks

Secondary

MeasureTime frame
1.Relieving of Mala sang and reduction in sign and symptoms of purishaja udavarta vyadhi 2.Effect of Eranda taila on gut biomarkersTimepoint: 3 weeks

Countries

India

Contacts

Public ContactDr Sachin Rangrao Patil

Bharati Vidyapeeth Deemed to be university College of Ayurved Pune

umesh.tekawade@bharatividyapeeth.edu9423210319

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026