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A study on the effectiveness of homoeopathic treatment for gout using the synthesis repertory

Clinical utility of the Synthesis Repertory in the treatment of Gout - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/07/113356
Enrollment
30
Registered
2026-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

None listed

Interventions

Intervention1: Individualized homoeopathic Drugs: Patient will receive Individualized homoeopathic treatment in a dosage of 3_5 globules per day,, frequency of 3 days in a duration of 6 Control Interv

Sponsors

Jsps Govt Homoeopathic Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patients who presented with symptoms and signs of gout, and diagnosed cases of both sexes, and those patients who expressed their willingness to participate in the study through a signed consent form

Exclusion criteria

Exclusion criteria: The study does not involve patients diagnosed with gout along with any serious systemic or pathological complications and advanced conditions, pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Clinical Understanding of Gout with Synthesis RepertoryTimepoint: 24 months—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactDRPGeorge Mullar

Jsps Govt Homoeopathic medical College

georgepatchigalla@gmail.com9000080662

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026