Comparative efficacy of nasal drops and orally oil administered in neck pain.

Efficacy of Nasya and Snehapana on Greevastambha with special reference to Cervical Spondylosis: An open-labelled randomized parallel group clinical trial.

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/05/052690

Enrollment

Registered

2023-05-16

Start date

Unknown

Completion date

Unknown

Last updated

2023-05-29

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

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients suffering from the classical sign and symptoms of cervical spondylosis. 2)Patients of either sex between the age group of 30 to 60 years. 3)Patients willing to provide written consent and able to participate in the study for 14 days and follow up for a period of 15 days. 4)Patient fit for Nasya Karma and Snehapana.

Exclusion criteria

Exclusion criteria: 1)Pregnant women and lactating mothers. 2)Patients suffering from uncontrolled systemic disorders such as Hypertension, Diabetes Mellitus and other systemic diseases which affect bones and joint conditions such as Rheumatoid arthritis. 3)Previous history of neck trauma, cervical fracture and surgery. 4)Cervical myelopathy.

Design outcomes

Primary

Measure	Time frame
Pain will be assessed through the Visual Analogue Scale.Timepoint: baseline day and after completion of trial	—

Secondary

Measure	Time frame
Changes in the following criterias- Neck disability index Range of movement Timepoint: baseline day and after completion of trial	—

Countries

India

Contacts

Public ContactDr Sarvesh Kumar Singh

National Institute of Ayurveda Jaipur

sarveshksingh21@gmail.com8739860237

Outcome results