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Study To Evaluate The Effect Of Terminalia Chebula In Patients With Irritable Bowel Syndrome

Effectiveness Of Terminalia Chebula In The Treatment Of Irritable Bowel Syndrome Using The Irritable Bowel Syndrome Symptom Severity Scale (IBS-SSS): An Interventional Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106610
Enrollment
34
Registered
2026-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Intervention1: Terminalia Chebula 30C: The Medicine Will Be Administered In Potentized Form In 30C Potency And The Route Of Administration Will Be Oral And At Baseline The Medicine Will Be Given As 4

Sponsors

National Institute Of Homoeopathy Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age group 18 to 50 years of both sexes Patients diagnosed with irritable bowel syndrome IBS as per Rome IV criteria 2016 Patients willing to participate by providing written informed consent

Exclusion criteria

Exclusion criteria: Patient associated with any other chronic and advanced systemic disease like uncontrolled Diabetes Mellitus Severe Hypertension Immunocompromised and Malignancy Patient taking treatment from any other system of medicine for same complaint Pregnant or lactating women Family history of colon cancer rectal bleeding age more than 50 years weight loss psychiatric conditions Any type of severe complication like fecal impaction rectal prolapse bowel leakage or surgical cases Patients with known hypersensitivity or allergy to Terminalia chebula or other Homoeopathic Medicine Systemic illness that required hospital admission Participation in any other clinical study during the study period

Design outcomes

Primary

MeasureTime frame
IRRITABLE BOWEL SYNDROME SYMPTOM SEVERITY SCALE (IBS- SSS)Timepoint: Assessed At Baseline And After 3 Months Of Intervention

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Manju Kumari

National Institute Of Homoeopathy Delhi

manju.nih@gov.in8375886140

Outcome results

None listed

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