A PRECLINICAL AND COMPARATIVE CLINICAL TRIAL OF VARMAM THERAPY WITH AND WITHOUT KURUNTHOTTI KASHAYAM (INTERNALLY) IN THE MANAGEMENT OF CEGANAVATHAM (CERVICAL SPONDYLOSIS)

National Institute of Siddha1 site in 1 country40 target enrollmentStarted: November 29, 2020Last updated: November 22, 2020

Conditions

Trial Snapshot

Phase: Phase 3
Status: Not yet recruiting
Sponsor: National Institute of Siddha
Enrollment: 40
Locations: 1
Primary Endpoint: UNIVERSAL PAIN ASSESSMENT SCALE

Study Overview Study Design Eligibility Criteria Outcomes Investigators Sites Records & Identifiers Similar Trials

Study Overview

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.

Study Design

Study Type: Interventional
Allocation: Computer generated randomization

Eligibility Criteria

Ages: 25.00 Year(s) to 55.00 Year(s) (—)
Sex: All

Inclusion Criteria

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

Exclusion Criteria

•Patient with uncontrolled hypertension 2.pregancy and lactation
•Cervical rib
•Spina bifida
•Ankylosis spondylosis
•Rheumatoid arthritis
•Patient with thyroid
•Any trauma history
•Loss of bowel and bladder control
•Dysphagia
•Fracture in neck region
•Coronary artery disease
•Tuberculosis
•Severe osteoporosis
•Neck surgery.

Outcomes

Primary Outcomes

UNIVERSAL PAIN ASSESSMENT SCALE

Time Frame: 48 days

Secondary Outcomes

To study the siddha basic principles relevant to the diseases(48 days)

Investigators

Sponsor

National Institute of Siddha

Sponsor Class

Research institution and hospital

Study Sites (1)

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