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A prospective open labelled clinical trial to assess the role of Homoepathic medicines in Cholelithiasis

A prospective open labelled clinical trial to assess the role of Homoeopathic medicines in Cholelithiasis - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093540
Enrollment
30
Registered
2025-08-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: K80- Cholelithiasis

Interventions

Intervention1: Homoeopathic medicines: Indicated homoeopathic medicine as per symptom similarity would be selected on the basis of totality of symptoms, followed by repertorization. Selected medicine

Sponsors

Director General, Central Council for Research in Homoeopathy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ? Patient with or without symptoms of upper abdominal pain and tenderness, nausea, vomiting, jaundice, or other dyspeptic features but having evidence of gallstones (single or multiple) or gall bladder sludge with average diameter less than or equal to 15 mm or showing contracted GB or partially contracted GB in Upper abdominal USG.

Exclusion criteria

Exclusion criteria: Complicated Cholelithiasis i.e. for example cases which need immediate surgical intervention and complications like obstructive jaundice perforation fistula empyema gangrene carcinoma liver failure cholangitis gallstone ileus or pancreatitis or any related serious complications. Acute cholecystitis with ASA classification greater than III Cirrhosis of Liver Malignancy Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
To evaluate the response of homoeopathic medicines by comparing the assessing status of Cholelithiasis (absent or present/ if still present _ increased, decreased or status quo) and gall bladder thickness via Upper abdominal USG at baseline, 6 months and 12 months and also assessing the symptoms of the patient via GSS (Gall stone symptom score)16at baseline, 3 months, 6 months, 9 months and 12 months.Timepoint: Baseline 6month 12month

Secondary

MeasureTime frame
To assess the quality of life using The Gastrointestinal Quality of Life Index (GIQLI) 17which includes both specific questions on gastrointestinal symptoms, for both the upper and lower digestive tracts, as well as generic questions on physical, emotional, and social capabilities and also comparing the parameters of LFT and Lipid profile (at baseline, 6 months, 12 months).Timepoint: Baseline 6month 12month

Countries

India

Contacts

Public ContactDrPartha Pratim Pal

Central Council for Research in Homoeopathy

justdoit.partha007@gmail.com8910890779

Outcome results

None listed

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