FindTrial
Sign In

Assessing the proneness & severity of vatarakta in specific Prakriti individuals

Assessment of Association between Prakriti and Vatarakta- A Cross-Sectional Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/05/053054
Enrollment
100
Registered
2023-05-23
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: M109- Gout, unspecified

Interventions

None listed

Sponsors

Ch Brahm Prakash Ayurved Charak Sansthan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Individuals aged 20 - 50 years of either gender 2. Individuals who consent in writing to participate in the study 3. Individuals presenting with clinical features of vatarakta, irrespective of gender and socio-economic status 4. Individuals presenting clinical features of gouty arthritis with hyperuricemia.

Exclusion criteria

Exclusion criteria: 1. Mentally unstable individuals 2. Individuals who have or have had a past history of a malignant tumor 3. Pregnant and lactating women 4. Individuals with autoimmune disorders of joints, infective and reactive arthritis 5. Individuals with severe toxicity, ulceration, progressive gangrenous changes.

Design outcomes

Primary

MeasureTime frame
Assessing vatarakta & its severity in specific Prakriti using sign & symptoms mentioned in classical text & using ACR/EULAR criteria then assessing Prakriti by using validated prakriti proforma.Timepoint: 15 days—

Secondary

MeasureTime frame
Determining the role of diet & lifestyle in prevention of vatarakta in various prakriti & designing treatment protocols.Timepoint: 15-365 days—

Countries

India

Contacts

Public ContactDr Sanju kumari

CBPACS

Alokayurlife@rediffmail.com8295438040

Outcome results

None listed

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