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Effect of Ayurvedic preparation Peedanil Gold with comparison to Yoga Module and Conventional care in Knee osteoarthritis patients

To Evaluate Efficacy of Peedanil Gold with Conventional Treatment and Yoga Module: A Three Arm, Randomized Control Trial in Knee Osteoarthritis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/01/039150
Enrollment
138
Registered
2022-01-05
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: M17- Osteoarthritis of knee

Interventions

None listed

Sponsors

Patanjali Research Institute Sponsored By Patanjali Research Foundation Trust
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age more than 40 years and less than 80 years Diagnosed case of knee Osteoarthritis according to NICE guidelines Onset of symptoms for more than 6 months Pain greater than 3 on numeric pain rating scale Grade greater than 1 on Kellgren and Lawrence Score Willing to participate and give consent for the study.

Exclusion criteria

Exclusion criteria: Patient with other inflammatory arthritic diseases like gout and rheumatoid arthritis Congenital dysplasia malignancy Knee surgery, or arthroscopy Intra articular injection of corticosteroid or chondroprotective drug in past 3 months of enrolment Serious acute systemic diseases Patient with recent knee injury Hip or knee replacement Asymptomatic patient Patient who cannot comply with intervention procedure Not willing to sign consent.

Design outcomes

Primary

MeasureTime frame
Clinically detectable changes in pain perception, severity of Osteoarthritis, changes in inflammatory biomarkers, functional improvementTimepoint: Baseline, 30 Days, and 60 Days. After initial 5 days of wash out period, baseline data will be collected.

Secondary

MeasureTime frame
Secondary: quality of life, fear of fall, Anxiety, sleep quality, treatment satisfaction.Timepoint: Baseline, 30 Days, and 60 Days. After initial 5 days of wash out period, baseline data will be collected.

Countries

India

Contacts

Public ContactKavita Bakshi

Patanjali Yog Gram, Haridwar

prinicipal.investigator@prft.in7302254793

Outcome results

None listed

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