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TO COMPARE THE EFFICACY OF ASHWAGANDHADYA GHRITA PANA AND NASYA ALONG WITH RASNAPANCHAK KWATHA AND GUGGULU VATI IN THE MANAGEMENT OF CERVICAL SPONDYLOSIS

A RANDOMISED COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFICACY OF ASHWAGANDHADYA GHRITA PANA AND NASYA ALONG WITH RASNAPANCHAK KWATHA AND GUGGULU VATI IN MANAGEMENT OF CERVICAL SPONDYLOSIS (GREEVA SANDHIGATAVATA) - CS

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/083350
Enrollment
40
Registered
2025-03-25
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Interventions

None listed

Sponsors

NATIONAL INSTITUTE OF AYURVEDA DEEMED TO BE UNIVERSITY DEEMED TO BE UNIVESRITY JAIPUR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either gender having age between 30-70 years 2. Patients with clinical signs and symptoms of Greeva sandhigata vata (Cervical Spondylosis) 3. Patients having a radiological finding of Cervical Spondylosis 4. Patients fit for Nasya karma and Snehapana

Exclusion criteria

Exclusion criteria: 1. Recent cervical, spinal, or shoulder trauma or surgery or any implantation in these sites 2. History of Cervical Spondylotic Myelopathy, Cervical Rib, severe Cervical Radiculopathy 3. Patients having systemic illness such as Ankylosing spondylitis, diffuse idiopathic skeletal hyperostosis, inflammatory arthritis 4. Patients having suspected TB or HIV infection, vascular insufficiency or malignancy 5. Pregnant or lactating women 6. Patients having known allergy to any of the trial drug

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study will be the change in Neck Disability Index ScoreTimepoint: At baseline and after four weeks

Secondary

MeasureTime frame
Secondary outcomes will include changes in scoring of subjective parameters assessing pain, neck stiffness and active neck movements (From baseline to the end of the treatment period)Timepoint: After four weeks

Countries

India

Contacts

Public ContactDR RASHMI MUTHA

NATIONAL INSTITUTE OF AYURVEDA, JAIPUR

rashmimutha21@yahoo.com7976512056

Outcome results

None listed

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