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To study the effects of ayurvedic treatment in the management of Cervical spondylosis

“A RANDOMIZED CONTROL CLINICAL TRIAL TO STUDY THE EFFECT OF AYURVEDIC TREATMENT PROTOCOL IN THE MANAGEMENT OF GREEVA SANDHIGATAVATA (CERVICAL SPONDYLOSIS) ?

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061218
Enrollment
40
Registered
2024-01-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: M478- Other spondylosis Health Condition 2: M478- Other spondylosis

Interventions

None listed

Sponsors

National Institute Of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.The patients having clinical signs and symptoms of Greeva Sandhigata Vata (Cervical Spondylosis). Pain must be an essential feature among all the features. 2.History of neck pain longer than 3 months. 3.The patients having chronicity of disease less than 5 years.

Exclusion criteria

Exclusion criteria: 1.History of neck trauma and fracture. 2.Recent cervical, spinal, or shoulder surgery or implanted instrumentation or previous surgery for cervical spondylotic myelopathy. 3.Known case of Intravertebral disc prolapse. 4.Patient participated in any clinical trial within last six months. 5.Known case of Inflammatory arthritic conditions like Rheumatoid arthritis, Ankylosing spondylitis and Malignancy, Tuberculosis ,HIV infection. 6.Patients who are having allergy to any trial drug. 7.Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
1.Changes in Visual Analogue Scale Pain score [change from pre- intervention to 2 weeks] Visual Analogue Scale pain score will be used to assess neck pain. Score ranges from 0-10. 0- shows least pain & 10- shows worst pain. Timepoint: 14 days

Secondary

MeasureTime frame
1.Changes in Universal Goniometer readings from pre-intervention baseline value at the end of 2 weeks 2.Changes in Neck Disability Index score from pre-intervention baseline value at the end of 2 weeks Timepoint: 30 days

Countries

India

Contacts

Public ContactANNU R

National Institute of Ayurveda , Jaipur.

rashmimutha21@yahoo.com7976512056

Outcome results

None listed

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