VARMAM THERAPY WITH AND WITHOUT KURUNTHOTTI KASHAYAM for the CEGANAVATHAM (CERVICAL SPONDYLOSIS)

Phase 3

Not yet recruiting

• Conditions: Other spondylosis with radiculopathy,

• Registration Number: CTRI/2020/11/029368
• Lead Sponsor: National Institute of Siddha

Brief Summary

This is the comparative two arm clinical study to evaluate the efficacy of varmam therapy with and without kurunthotti kashayam in the management of ceganavatham in 40 patients for 48 days. The outcome will be measured by Universal pain scale and reduction in clinical symptoms.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2020-11-22
• Study Start: 2020-11-29

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Pain present behind the neck Region, aggravated by movement 2.
• Neck stiffness 3.
• Difficulty in flexion and extension of neck 4.pain radiating to shoulder blade, top of the shoulder, upper arm and back of the head 5.
• Dizziness or vertigo 6.
• Numbness in both upper limb 4.
• Pain radiating to.

Exclusion Criteria

• Patient with uncontrolled hypertension 2.pregancy and lactation 3.
• Cervical rib 4.
• Spina bifida 5.
• Ankylosis spondylosis 6.
• Rheumatoid arthritis 7.
• Patient with thyroid 8.
• Any trauma history 9.
• Loss of bowel and bladder control 10.
• Dysphagia 11.
• Fracture in neck region 12.
• Coronary artery disease 13.
• Tuberculosis 14.
• Severe osteoporosis 15.
• Neck surgery.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
UNIVERSAL PAIN ASSESSMENT SCALE	48 days

Secondary Outcome Measures

Name	Time	Method
To study the siddha basic principles relevant to the diseases	48 days

Trial Locations

Locations (1)

Ayothidoss pandithar hospital; 🇮🇳 Kancheepuram, TAMIL NADU, India

Ayothidoss pandithar hospital

🇮🇳Kancheepuram, TAMIL NADU, India

Dr D Krishnapriya

Principal investigator

8012634515

krishnadoss14@gmail.com