A clinical trial to study the effect of two oil nasya, Prabhanjanavimaradana Taila and Tila taila in patients with cervical spondylosis

â??Double-blind comparative clinical study on Prabhanjanavimardana Taila and Tila taila Nasya in Vishwachiâ?? - PAT

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/02/023182

Enrollment

Registered

2020-02-07

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: M472- Other spondylosis with radiculopathy

Interventions

Intervention1: Prabhanjanvimardana Taila: Each patient will be subjected to Prabhanjanavimardana Taila Nasya 4ml in each nostril once a day for 7 days Control Intervention1: Moorchita Tila Taila: Each

Eligibility

Inclusion criteria

Inclusion criteria: Patients with symptoms of Vishwachi between age group 30 - 70 years of either sex. Patients who are fit for Nasya Karma.

Exclusion criteria

Exclusion criteria: Patients with the history of recent trauma, congenital anomalies of cervical spine. Patients contra-indicated for Nasya karma.

Design outcomes

Primary

Measure	Time frame
Neck pain Neck stiffness Tingling sensation Neck disability index17 Tenderness on neck and upper limb Range of movement Timepoint: 2 months	—

Secondary

Measure	Time frame
Not applicableTimepoint: Not applicable	—

Countries

India

Contacts

Public ContactDr Llifam Roshanara

ALVAâ??S AYURVEDA MEDICAL COLLEGE AND HOSPITAL

vikramkumar83@gmail.com9483141326

Outcome results

None listed

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