Skip to content

Effect of Gokshuradi Guggulu in Gout

A COMPARATIVE CLINICAL STUDY OF GOKSHURADI GUGGULU WITH ANUPANA BHEDA IN THE MANAGEMENT OF VATARAKTA W.S.R. TO GOUT - GAVG

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/03/008106
Enrollment
40
Registered
2017-03-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- patient having sign and symptoms of vatarakta(gout)

Interventions

Intervention1: Gokshuradi Guggulu with Lukewarm Water: Gokshuradi Guggulu 1gm BD with lukewarm water as anupana
route of administration-orally
time duration-60 days. Control Intervention1: Gokshuradi guggulu with guduchi kwatha: Gokshuradi Guggulu 1gm BD per orally with guduchi kwatha as anupana in group 2 for 60 days in both groups

Sponsors

Desh Bhagat Ayurvedic college and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a) Patients willing for trial. b) Patients of age group between 16-70 years irrespective of sex. c) Patients having clinical signs and symptoms of Vatarakta. d) Patients having serum uric acid level 6 mg/dl with associated features like joint pain and inflammation. e) Not having any state mentioned in exclusion criteria.

Exclusion criteria

Exclusion criteria: a) Patients not willing for the trial. b) Patients below age of 16 years and above 70 years of age. c) Any other joint inflammatory disorder like RA. d) Uncontrolled Diabetes and Hypertension. Chronic renal disease. e) Patients having chronicity more than 10 years. f) Disease associated with marked joint destruction. g) Hemarthrosis, Koch arthritis, Septic arthritis. h) Severe multi organ syndromes. i) Patients suffering from major systemic illness. j) Pregnant and lactating women. k) Any other state thought fit for exclusion.

Design outcomes

Primary

MeasureTime frame
The improvement was assessed on the basis of relief found in the cardinal symptoms of the disease. To assess the effect of therapy objectively, all the sign and symptoms were given scoring pattern depending upon their severityTimepoint: 60 days

Secondary

MeasureTime frame
The improvement was assessed on the basis of relief found in the cardinal symptoms of the disease. To assess the effect of therapy objectively, all the sign and symptoms was given scoring pattern depending upon their severityTimepoint: 60 days

Countries

India

Contacts

Public ContactDrRimpaljeet Kaur

P G School Of Ayurveda and Research

dr.rimpal@gmail.com9988180021

Outcome results

None listed

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