Skip to content

Effectiveness of an Ayurvedic formulation in Ulcerative colitis(Pittaja Atisara).

Exploring the Disease Modifying Potential of an Ayurvedic Formulation in Ulcerative Colitis (Pittaja Atisara): An Experimental and Clinical Study - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/086075
Enrollment
20
Registered
2025-04-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: K519- Ulcerative colitis, unspecified

Interventions

None listed

Sponsors

Institute of Post Graduate Ayurvedic Education and Research at SVSP Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Only the patients with positive colonoscopic finding of ulcerative colitis will be included in the present clinical study. 2.History of passing of bloody stool or diarrhea mixed with blood and mucus. 3.Bleed on rectal examination. 4.Abdominal pain. 5.Increase of abdominal sound. 6.Malnutrition. 7.Weight loss. 8.Participants should have signed informed consent letter.

Exclusion criteria

Exclusion criteria: 1.Pregnant or planning for pregnancy, breastfeeding mother 2.Enrolled in other clinical trials 3.Have active malignancy or are under investigation for malignancy Have a history of any of the following medical conditions- Cushing syndrome, HIV, Chronic kidney disease(CKD), Chronic liver disease(CLD),Hematemesis Currently taking any of the following medication- Alcohol or drug abuse, psychiatric medication, oral steroid.

Design outcomes

Primary

MeasureTime frame
The primary outcome will be measured based on clinical outcome, colonoscopic outcome, Hematological and biochemical outcome, fecalysis outcome measures including OBT to determine the effectiveness and safety of the test drug for the Treatment of Ulcerative colitis(Pittaja Atisara).Timepoint: 8 weeks

Secondary

MeasureTime frame
The Effect of the test drug medication alters the quality of the life that will be evaluated after completion of the treatment.Timepoint: 8 weeks

Countries

India

Contacts

Public ContactJalal Miah

Institute of Post Graduate Ayurvedic Education and Research at SVSP Hospital

atipgaer@gmail.com9874849650

Outcome results

None listed

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