Skip to content

To Study The Effect Of Kaishora Guggulu In Vatarakta (Gout) With Investigation Of Serum Uric Acid.

Randomized controlled clinical trial to study effect of Kaishora Guggulu in vatarakta (Gout) with special reference to serum uric acid. - vatarakta

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/105086
Enrollment
60
Registered
2026-02-27
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: PCS-

Interventions

None listed

Sponsors

Dr Snehal Uttamrao Ranvir
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patient having sing and symptoms such as Sandhishoola, Sprashasahatva,Sandhishotha Stabdhata, Daha. patient of either gender,irrespective of socioeconomic status

Exclusion criteria

Exclusion criteria: patient below 18 years and above 60 years old. pregnant women and lactating mother. knowncase of HIV. knowncase Rheumatoid arthritis, Tubercular arthritis Syphilitic arthritis, Maleria, Neurological disorder. knowncase of chikungunya knowncase of erythematous. serum uric acid level more than 12mg/dl.

Design outcomes

Primary

MeasureTime frame
to study add on effect of kaishora guggulu in the management of vatarakta (gout) with special reference to serum uric acidTimepoint: 30 days

Secondary

MeasureTime frame
1)To study vatarakta in detail according to ayurveda 2)To study gout in detail according to modern science 3) To study kaishora guggulu properties. 4)To study serum uric acid in details. 5)To study effect of kaishora guggulu on sign & symptoms of vatarakta & on uric acid levels.Timepoint: 18 months

Countries

India

Contacts

Public ContactDr Gauri Atmaram Mulik

LRP Ayurvdic Medical College And Hospital Post Graduate Institute and Research Center Islampur

gaurimohite492@gmail.com8806073556

Outcome results

None listed

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