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Effect of Valuka Pinda Sweda in Manyastambha (Cervical Spondylosis)

A randomized controlled clinical trial to study the adjuvant effect of valuka pinda sweda with isometric neck exercises in manyastambha with special reference to cervical spondylosis - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088346
Enrollment
76
Registered
2025-06-05
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Dr Sneha Nikam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients having classical signs and symptoms of Manyastambha like stiffness and pain in the neck region. 2) Patients fulfilling the diagnostic criteria. 3) Patient who will give consent & Fit for the procedure.

Exclusion criteria

Exclusion criteria: 1)Patients with history of fracture or dislocated of cervical region. 2)Patients with Diabetes and Cardio vascular diseases, traumatic, infective, neoplastic spine. 3) Known case of Congenital anomalies of spine. 4)Patients having automotive deformities like ankylosing spondylitis, spinal cord abscess, Rheumatoid arthritis as well as congenital structural disorder will be excluded. 5) Traumatic disorders like cervical strain, injuries to intervertebral joints, ligaments and muscles, Fractures and ruptured disc. 6) Patients with other joints disorder which are not relates to Manyastambha will be excluded.

Design outcomes

Primary

MeasureTime frame
Reduction in signs and symptoms of ManyastambhaTimepoint: 7 days

Secondary

MeasureTime frame
Where the trial group stands in comparison with control groupTimepoint: 18 months

Countries

India

Contacts

Public ContactDr Sneha Dhananjay Nikam

SMBT Ayurved College and Hospital

vdpramod31@gmail.com9604633832

Outcome results

None listed

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