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Clinical Trials/CTRI/2024/05/067683
CTRI/2024/05/067683
Not Yet Recruiting
N/A

An Observational study to evaluate the impact of Ayurvedic whole system and personalized management in selected cases of Amavata who have been previously treated with standard modern care. - NI

State Ayurvedic College and Hospital Lucknow0 sites0 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Health Condition 1: M059- Rheumatoid arthritis with rheumatoid factor, unspecified
Sponsor
State Ayurvedic College and Hospital Lucknow
Status
Not Yet Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational

Investigators

Sponsor
State Ayurvedic College and Hospital Lucknow

Eligibility Criteria

Inclusion Criteria

  • 1\. Patients coming to Kayachikitsa OPD, State Ayurvedic College, Lucknow having joint symptoms clinically diagnosable as amavata, for not less than 6 months.
  • 2\. Patients previously diagnosed for having Rheumatoid Arthritis (ACR 2010 criteria) and having been treated through standard modern care for not less than 3 months under the supervision of a qualified rheumato\-logist/clinical immunologist/ orthopedic surgeon/ neurologist or a specialist physician.
  • 3\.Minimum 6 joints (swollen or tender) involved at the time of registration in the study.
  • 4\.Patients having concerns about their ongoing modern care for joint disease and are willing to take ayurvedic therapy either in continuation with ongoing modern treatment or are willing to reduce or stop the modern medication. This also includes the patients who have stopped their modern medication at their own long back.

Exclusion Criteria

  • 1\.Patient with chronic rheumatoid arthritis having developed joint deformities
  • 2\.Patients having additional joint pathologies (Gout/OA) besides having RA.
  • 3\.Patients currently or previously (in past three months) on steroid therapy.
  • 4\.Patients who were on some Ayurvedic therapy in past 3 months.
  • 5\.Patients having impaired renal or hepatic function
  • 6\.Pregnancy and lactation

Outcomes

Primary Outcomes

Not specified

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