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A comparative clinical study to assess the efficacy of Prasaraini taila administered nasally in the morning in one group and evening in the other group in cervical spondylosis

An open label comparative clinical study to evaluate the efficacy of nasya karma performed in pratahkala and sandhyakala in viswachi w.s.r to cervical spondylosis - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/113006
Enrollment
40
Registered
2026-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: M479- Spondylosis, unspecified

Interventions

None listed

Sponsors

Dr Geeta Patel
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects presenting with clinical features of Cervical spondylosis of either gender between the age group of 20 to 60 years will be selected Subjects fit for Nasya Karma will be selected

Exclusion criteria

Exclusion criteria: Subjects presenting with the history of any major systemic disorders that may interfere with the course of treatment Subjects presenting with dislocation or fracture of cervical spine

Design outcomes

Primary

MeasureTime frame
To evaluate and compare the therapeutic effectiveness of Nasya Karma administered during Pratahkala and Sayankala in the management of Cervical Spondylosis with respect to clinical improvement and symptom reliefTimepoint: 1 year 2 months—

Secondary

MeasureTime frame
NilTimepoint: Not Applicable—

Countries

India

Contacts

Public ContactDr Geeta Patel

Sri kalabyraveshwara swamy ayurvedic college hospital and research center

shreyasdmbams@gmail.com9880920154

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026