To evaluate the combined effect of prasarini taila pratimarsha nasya and prsarini capsule in cervical radiculopathy

Phase 1

Not yet recruiting

• Conditions: Cervical disc disorder with radiculopathy. Ayurveda Condition: VISVACI,

• Registration Number: CTRI/2025/03/083705
• Lead Sponsor: SDM College Of Ayurveda and Hospital

Brief Summary

The Study title is An Open Label Single Arm Clinical Study On The Combined Effect Of Prasarini Taila Pratimarsha Nasya And Prasarini Capsule In Vishwachi [Cervical Radiculopathy] which involves a total of 30 participants in the study, which includes age from 30years to 60 years and up-to 1 year chronicity and study excludes known cases of traumatic injury of cervical spine , cervical fracture , uncontrolled cases of diabetes mellitus and hypertension, and pregnant women and lactating women, assessment will be doe on 0th, 11th and 22nd day after treatment and results of the following study will be analysed and calculated by using SPSS and other suitable statistical software.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2025-03-27
• Study Start: 2025-10-04

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Chronicity upto 1 year.
• Subjects who are fit for nasya.
• Subjects irrespective of gender, caste, creed, occupation, religion and socio-economic status.
• Subjects who are willing to participate and ready to sign the informed consent form.

Exclusion Criteria

• Known cases of traumatic injury of cervical spine , cervical fractures, cervical myelopathy.
• Known uncontrolled cases of diabetes mellitus and hypertension.
• Impaired cardiac , renal and hepatic functions, known cases of neoplasm and infective disorders.
• Pregnant women and lactating mothers.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Restricted movement of neck and shoulder joint	0th day , 11th day and 22nd day
2. Radiating pain from nape of the neck, shoulder down to the arm	0th day , 11th day and 22nd day
3. Spurling test	0th day , 11th day and 22nd day
4. Visual analogue scale of pain	0th day , 11th day and 22nd day

Secondary Outcome Measures

Name	Time	Method
Quality of life WHO	0th, 11th & 22nd day

Trial Locations

Locations (1)

Sri Dharmasthala Manjunatheshwara College Of Ayurveda And Hospital Hassan; 🇮🇳 Hassan, KARNATAKA, India

Sri Dharmasthala Manjunatheshwara College Of Ayurveda And Hospital Hassan

🇮🇳Hassan, KARNATAKA, India

Dr Rakshitha J

Principal investigator

9900744890

jrachu59@gmail.com