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A Pharmaco clinical study of effect of Ashwagandha Ghrita and Bala tail in knee osteoarthritis

A Pharmaco clinical Study To Evaluate The Efficacy Of Ashwagandha Ghrita (Withania somnifera Linn) and Bala Tail(Sida cordifolia Linn) in Janu Sandhivata wsr to Knee Osteoarthritis - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092323
Enrollment
60
Registered
2025-08-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

None listed

Sponsors

State Ayurvedic College and Hospital, Lucknow
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Age group between 40 to 70 years 2 The patients with classical signs and symptoms of sandhivata given in various texts as well as the clinical features of disease of OA given in Modern medicine 3 Patient who gave the consent to participate in study

Exclusion criteria

Exclusion criteria: 1 Age group less than 30 years and more than 70 years 2 Patients having past history or actively suffering from other inflammatory disease like RA Gout Septic Arthritis etc 3 Cases with severe deformities of joint and having major complications are excluded 4 Pregnant and lactating women 5 Patients having substantial abnormalities in Hematological Hepatic Metabolic function and systemic disorders like Diabetes and Hypertension 6 Avaranjanya Sandhivata

Design outcomes

Primary

MeasureTime frame
1. pain in joints 2. crepitus 3. pain during extension and flexion 4. loss of motion and range 5. swelling in affected joint 6. morning stiffness(less than half an hour) 7. tenderness of jointTimepoint: - the follow up conducted during study period for once in 15 days. After completion of trial of two month, the follow up without drug after 15th day

Secondary

MeasureTime frame
1. CBC, ESR 2. Blood sugar (HbA1c/random/fasting/pp) 3. CRP, Sr. Uric acid, RA factor 4. Lipid profile, LFT, KFT 5.X-Ray of the affected joint- AP/lateral view 6. S. Calcium, Vit. D3, thyroid profile, bone mineral density (if necessary)Timepoint: - the follow up conducted during study period for once in 15 days. After completion of trial of two month, the follow up without drug after 15th day

Countries

India

Contacts

Public ContactProf R B Yadav

State Ayurvedic College and Hospital, Lucknow

drrby67@gmail.com9412196868

Outcome results

None listed

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