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Comparative clinical study of pathyadi churn and erand tail in Aamvat (joint related disorder)

Phase 1
Conditions
Health Condition 1: M057- Rheumatoid arthritis with rheumatoid factor without organ or systems involvement
Registration Number
CTRI/2024/03/063710
Lead Sponsor
Department of Kayachikitsa Faculty of Ayurveda
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients willing to participate for this trial. Diagnosed cases of Amavata based on symptoms and signs described in Madava Nidana & ACR-EULAR 2010. Sero positive &Sero negative both cases are included.

Exclusion Criteria

Not willing patients.

Patients with short history of less than a year. Patients having severe deformities.

Patients of Gouty Arthritis, Septic Arthritis, Osteoarthritis, Ankylosing Spondylitis.

HIV, Tuberculosis, Hypertension, D.M., & other systemic problems.

? Pregnant & lactating women

? Patients with major complications are like pleural effusion, ascites also excluded.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
A) Pain <br/ ><br>B) TENDERNESS <br/ ><br>C) MORNING STIFFNESS <br/ ><br>D) SWELLING OVER JOINTS <br/ ><br>E) FUNCTIONAL ASSESSMENT: <br/ ><br>F) WALKING TIME <br/ ><br>G) GRIP POWER & PRESSING POWER <br/ ><br>H) RANGE OF MOTIONTimepoint: 90 days study with follow-up of every 30 days
Secondary Outcome Measures
NameTimeMethod
a. Laboratory Investigations- <br/ ><br>b. Hematological—Hb%, TLC, DLC, ESR <br/ ><br>c. Biochemical—LFT, RFT, Lipid Profile, Blood Sugar. <br/ ><br>d. Anti CCP antibodies(immunopathological marker) <br/ ><br>e. RA factor Quantitative, CRP Quantitative <br/ ><br>f. ASO –titreTimepoint: 90 days study with follow-up of every 30 days
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