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A Clinical Study on Arthritis.

A Comparative Clinical Study to Evaluate the Efficacy of Shaman Yoga and Saindhavadi Taila Matra Vasti in the Management of Amavata w.s.r. Rheumatoid Arthritis

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/08/009423
Enrollment
45
Registered
2017-08-21
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Amavata (Rheumatoid arthritis)

Interventions

Intervention1: Hingwadi Churna 2.Rasna â??Dashmula Kwatha: 1.Hingwadi Churna - 5 gm b.d. with lukewarm water 1 hour before meal. 2.Rasna â??Dashmula Kwatha- 40 ml b.d. 1 hour after meal. Control Inter

Sponsors

Rishikul Campus Haridwar UAU
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients having classical features of Amavata. Age group of 18-60 years. Patients fulfilling American College of Rheumatology (ACR) criteria, 1987. Both sero -positive and sero- negative cases were included in present study.

Exclusion criteria

Exclusion criteria: Chronicity for more than 15 years. Having severe crippling deformity. Patients with other systemic diseases like Cardiac disease, Tuberculosis, Diabetes mellitus, Hypertension. Any other serious medically and surgically ill patients.

Design outcomes

Primary

MeasureTime frame
To assess the effect of therapy subjectively and objectively, all the signs and symptoms were given scoring depending upon their severity. The result thus obtained from individual patient was categorized as: Excellent â?¥75% relief Marked Improvement â?¥50% up to 74% relief Mild improvement â?¥25% up to 49% relief No improvement â?¤24% relief Timepoint: 60 days

Secondary

MeasureTime frame
Exacerbations in sign and symptomsTimepoint: 1 month

Countries

India

Contacts

Public ContactArchana Negi

Rishikul Campus, Haridwar, UAU

archananegi89@gmail.com8958901101

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026