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Homoeopathic treatment of irritable bowel syndrome

A mixed-method research to develop diagnostic criteria for tubercular diathesis in homoeopathy and its use in a subsequent double-blind, randomized, placebo-controlled trial evaluating the efficacy of homoeopathic medicines in irritable bowel syndrome - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064838
Enrollment
82
Registered
2024-03-27
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Sponsors

The Calcutta Homoeopathic Medical and College Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age range: between 18-65 years 2. Either sex or transgender. 3. The patients suffering from IBS (ICD-10- CM K58.0) as per Rome IV diagnostic criteria, i.e., recurrent abdominal pain on average of at least 1 day/ week in the last 3 months associated with either of the following criteria related to defecation, associated with a change in frequency of stool and or associated with a change in form of appearance of stool 4. Patient willingness and written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients not providing with informed consent voluntarily. 2. Diagnosed cases of unstable psychiatric complaints or systemic diseases affecting quality of life. 3. Major gastro-intestinal surgery in last 6 months 4. For any chronic condition(s), pregnant, lactating and puerperal women 5. Currently ongoing usual standard therapy for IBS 6. Self-reported immune compromised conditions. 7. Substance abuse or dependence. 8. Vulnerable population–Unconscious, non-ambulatory, to oil for consultation, differently abled, terminally ill or critically ill patients, mentally disabled people 9. Undergoing homoeopathic treatment for any chronic disease within last 6months 10. Simultaneous participation in any other clinical trial

Design outcomes

Primary

MeasureTime frame
Irritable Bowel Syndrome Quality of Life Questionnaire (IBS-QOL)Timepoint: Every month up to 3 months

Secondary

MeasureTime frame
Irritable Bowel Syndrome Symptom Severity Score(IBS-SSS)Timepoint: Every month up to 3 months;Measure Yourself Medical Outcome Profile (MYMOP2)Timepoint: Every month up to 3 months

Countries

India

Contacts

Public ContactRajat Chattopadhyay

The Calcutta Homoeopathic Medical College and Hospital

dr.rajatchatterjee@gmail.com9331041142

Outcome results

None listed

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