Skip to content

yurveda-Based Enema to Support People with Irritable Bowel Syndrome.

A Single Arm Clinical Study to Assess the efficacy of Priyangvadibasti in Grahanidosha with Special Reference to Irritable Bowel Syndrome. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085032
Enrollment
30
Registered
2025-04-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: K582- Mixed irritable bowel syndrome

Interventions

None listed

Sponsors

National Institute of Ayurveda Deemed University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients suitable for Basti Karma Patients of either sex in the age group of above 18 years and below 60 years. Patient with classical signs and symptoms of Grahani (~IBS), i.e. Muhur Baddha/Drava Mala Pravritti, Picchila/Durgandhit Mala Pravrittu, Vidaha etc Uncomplicated cases with classical pictures of Grahanidosha will be selected irrespective of sex, caste, religion and profession

Exclusion criteria

Exclusion criteria: Patient having age below 18 years and above 60 years. Patients suffering from Acute Diarrhea, Gastric and Peptic Ulcers, uncontrolled D.M. and H.T. Patients with bleeding per rectum. Pregnant and lactating women. Mixed infection with parasites like round worms, hook worms etc. Patients with evidence of malignancy. Ulcerative colitis, Malabsorption syndrome, I, Intestinal tuberculosis. Patients suffering from major systemic illness like cancer, crohn s disease, renal failure. Patients who are taking corticosteroids, antidepressants, anticholinergic, or any other drugs that may have an influence on the outcome of study. Alcoholics and drug abusers. Other chronic debilitating disease like STD etc Patients who have completed participation in any other clinical trial during the past six months

Design outcomes

Primary

MeasureTime frame
Change in sign and symptoms of disease like Muhur Baddha, Muhur Drava Malapravritti, Ama etcTimepoint: Day 0 and Day 23 and Day 53

Secondary

MeasureTime frame
Change in Urine R/M, LFT, ESR.Timepoint: Day 0 and Day 23 and Day 53

Countries

India

Contacts

Public ContactDr Fatemeh Moazzamipeiro

National Institute Of Ayurveda Deemed University

guptadr.nisha@gmail.com9828087640

Outcome results

None listed

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