Skip to content

Healthy Diet and Yoga for Grahani Roga(Irritable Bowel Syndrome)

Effect of Pathya-Apathya and selected Yogic Practices in the Management of Grahani Roga with special reference to Irritable Bowel Syndrome - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101804
Enrollment
90
Registered
2026-01-22
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: K929- Disease of digestive system, unspecified

Interventions

None listed

Sponsors

Department of Swathavritta and Yoga Faculty of Ayurveda
Lead Sponsor
Department of Gastroenterology
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with clinical features of Grahani Roga 2.Patients diagnosed with IBS, based on Rome IV criteria or a similar standard diagnostic guideline 3.Inclusion of specific IBS subtypes IBS-D (diarrhoea predominant) 4.Patients with mild to moderate IBS severity, measured by a validated scale of IBS Severity Scoring System (IBS-SSS) 5.Patients willing to participate in the study

Exclusion criteria

Exclusion criteria: 1.Individuals with severe IBS symptoms that may require immediate medical intervention 2.Pregnant or breastfeeding women 3.Patients with other GI diseases (e.g., inflammatory bowel disease, celiac disease, colorectal cancer) 4.Severe psychiatric illnesses (e.g., major depression, schizophrenia) 5.Patients with diabetes, cardiovascular disorders, thyroid and renal diseases or any other systemic diseases 6.Patients already following specific diets (e.g., low FODMAP, gluten-free) 7.Recent use of antibiotics or probiotics within the past 4-6 weeks 8.Participants enrolled in any other clinical trials that may affect outcomes

Design outcomes

Primary

MeasureTime frame
Expected Reduction in Symptoms Severity Scale, BMITimepoint: Follow up of patients of all 3 groups will be done at an interval of every one month, for total study period of 3 months

Secondary

MeasureTime frame
Expected Improvement in Quality of Life, Perceived Stress Scale, Agni BalaTimepoint: Follow up of patients of all 3 groups will be done at an interval of every one month, for total study period of 3 months

Countries

India

Contacts

Public ContactDr Devesh Prakash Yadav

Banaras Hindu University Varanasi

nathanineeru1@gmail.com9454187783

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026