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Clinical Trials/CTRI/2023/05/053054
CTRI/2023/05/053054Not yet recruitingNot Applicable

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

Ch Brahm Prakash Ayurved Charak Sansthan1 site in 1 country100 target enrollmentStarted: May 31, 2023Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
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.
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

This  is an observational type of study assessing the association between types of Prakriti & vatarakta w.s.r to severity of vatarakta in specific Prakriti. This study will be conducted for a time period of one year in CBPACS with outcome of specifically designed diet & lifestyle, treatment protocols, and with the prevalence of vatarakta being  studied in different Prakriti subjects preventive measures could also be taken.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
20.00 Year(s) to 50.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •Individuals aged
  • •50 years of either gender
  • •Individuals who consent in writing to participate in the study
  • •Individuals presenting with clinical features of vatarakta, irrespective of gender and socio-economic status
  • •Individuals presenting clinical features of gouty arthritis with hyperuricemia.

Exclusion Criteria

  • •Mentally unstable individuals
  • •Individuals who have or have had a past history of a malignant tumor
  • •Pregnant and lactating women
  • •Individuals with autoimmune disorders of joints, infective and reactive arthritis
  • •Individuals with severe toxicity, ulceration, progressive gangrenous changes.

Outcomes

Primary Outcomes

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.

Time Frame: 15 days

Secondary Outcomes

  • Determining the role of diet & lifestyle in prevention of vatarakta in various prakriti & designing treatment protocols.(15-365 days)

Investigators

Sponsor
Ch Brahm Prakash Ayurved Charak Sansthan
Sponsor Class
Government medical college

Study Sites (1)

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