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Clinical Trials/CTRI/2010/091/006125
CTRI/2010/091/006125
Completed
Phase 2

A pilot study to evaluate the therapeutic efficacy of Siddha herbo mineral formulations Chandamarutha Chenduram (Internal) and Poonaga thylam (External) in the treatment of Uthiravatha suronitham (Rheumatoid arthritis)

ational Institute of Siddha Chennai Tamil Nadu India0 sites40 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
ational Institute of Siddha Chennai Tamil Nadu India
Enrollment
40
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
ational Institute of Siddha Chennai Tamil Nadu India

Eligibility Criteria

Inclusion Criteria

  • Age: 15\-60 years,
  • Sex: Both male and female
  • Patients having the symptoms of arthritis of three or more joints, symmetrical joint involvement, swelling especially in inter phalangeal joints, morning stiffness of joints, low grade fever, serum rheumatoid factor both positive and negative, anorexia \& mental stress
  • Patients who are willing to give radiological investigation and provide blood for lab investigation
  • Patient willing to sign informed consent stating that he/she will conscientiously stick to the treatment during 48 days but can opt out of the trial of his/her own conscious discretion

Exclusion Criteria

  • Cardiac disease
  • Hypertension
  • Diabetes mellitus
  • Use of narcotic drugs
  • Pregnancy and lactation
  • History of trauma
  • Tuberculosis
  • Bronchial asthma
  • Any other serious illness

Outcomes

Primary Outcomes

Not specified

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