A clinical trial to study the effect of trial drug MATHIYOOSHNA RASAYANAM(Internal),NYMPATHY THYLAM(External)on UTHIRAVATHA SURONITHAM (Rheumatoid Arthritis).

Phase 2

Recruiting

• Conditions: Pain in all major and minor joints swelling of jointsmorning stiffness more then one hour

• Registration Number: CTRI/2018/02/012040
• Lead Sponsor: Dr S Neelavathi

Brief Summary

Phase IIcriteria based clinical study to evaluate the clinical efficacy of siddha herbomineral formulation ofMathiyooshna Rasayanam(Internal) 6.002gram Bd andNympathy Thylam 30 ml (External) on UTHIRAVATHASURONITHAM (Rheumatoid Arthritis) for 40 daysin 40 patients during the trial period of 1 year 6 months that will beconducted in government siddha medical college palyamkottai tamil nadu theprimary out come is Reducing the pain and weakness by the trail drug Mathiyooshna Rasayanam (Internal) and Nympathy Thylam  (external) the secondary outcome will be the Evaluation of siddha diagnosticparameters.

Detailed Description

Not available

Study Timeline

• Study Start: 2017-05-09
• Last Update Posted: 2018-02-22

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Symmetrical joint involvement Arthritis of 3 or more joints.
• Rheumatoid factor positive or negative Morning stiffness.
• Swelling especially in the inter phalangeal joint.
• Patients who are willing for admission and stay in IPD for 40 days or willing to attend OPD Patient who is willing to undergo radiological investigation and give blood and urine samples for laboratory investigation.
• Patient willing to sign the informed consent stating that he/she will consciously stick to the treatment during 40 days but can OPD out of the trial of his/her own conscious discretion.

Exclusion Criteria

Systemic illness Pregnancy and lactation History of trauma Neurological disorder Tubercular arthritis Any other serious illness Psoriatic arthritis Gouty arthritis.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reducing the pain and weakness	40 days

Secondary Outcome Measures

Name	Time	Method
Evaluation of Siddha Diagnostic Parameters	40 days

Trial Locations

Locations (1)

Government Siddha Medical College; 🇮🇳 Tirunelveli, TAMIL NADU, India

Government Siddha Medical College

🇮🇳Tirunelveli, TAMIL NADU, India

Dr S Aysha

Principal investigator

8428621182

aysha.mdsiddha@gmail.com