A study of Prasrini taila administration through nasal and through anus in treatment of Cervical spondylosis.

Phase 3

Not yet recruiting

• Conditions: Other spondylosis,

• Registration Number: CTRI/2018/10/015990
• Lead Sponsor: National Institute of Ayurveda Jaipur

Brief Summary

The trial is an open label randomized clinical trial. The primary aim of the trial is to compare the efficacy of Nasya Karma(nasal administration) with Prasarini Taila(oil) and efficacy of Matra Basti (anal administration)of Prasarini Taila ( oil) in the management of  Greevastambh  w.s.r. to Cervical Spondylosis. Total 60 patient will be taken for trial. The patient will be randomly divided into two groups of 30 patients each. In group A Nasya Karma with Prasarini  taila in the dose of 8 drops (6ml) in each nostril will be done for 14 days .In group B  Matra Basti( anal administration ) of Prasarini  taila in the dose of 75ml  once a day for 14 days . The primary outcome will be the improvement in  total score of mJOA and range of motion.The patient will be  finally assessed after 45 days  of treatment.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2018-09-10
• Study Start: 2019-01-01

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• (1)Patients with features of Greevastambh (Cervical spondylosis) (2)Patients fit for Nasya and Matra Basti.
• (3)Patients having sign and symptoms supported by X-ray findings as per Visual Analog Scale, Modified Japanese Orthopedic Score).

Exclusion Criteria

• (1)Patients suffering from rheumatoid arthritis, gout, ankylosing spondylitis.
• (2)Patients with major systemic disorders.
• (3)Patients with stenosis of spinal canal, myelopathy.
• (4)Pregnant women and lactating mother.
• (5)Patients with any surgical history at cervical region.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
changes in modified Japanes orthopaedic association score (mJOA score) and range of movement	45 days

Secondary Outcome Measures

Name	Time	Method
changes in VAS score and global assessement of disease activity.	45 days

Trial Locations

Locations (1)

National Institute of Ayurveda, Jaipur; 🇮🇳 Jaipur, RAJASTHAN, India

National Institute of Ayurveda, Jaipur

🇮🇳Jaipur, RAJASTHAN, India

Dr Sarvesh Kumar Singh

Principal investigator

8739860237

sarveshksingh21@gmail.com