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To study the effect of Ayurvedic treatment in the improvements of patients with Cervical Spondylitis.

To study the Safety and Efficacy of classical Ayurvedic treatment in the functional improvements of patients with Cervical Spondylitis - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/060046
Enrollment
30
Registered
2023-11-21
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M452- Ankylosing spondylitis of cervicalregion

Interventions

Intervention1: Kshirbala oil: 10-20 ml to be massaged on affected area once a day for 14 days. Control Intervention1: Standard Kshirbala Oil: 10-20 ml to be massaged on affected area once a day for 14

Sponsors

Mprex Healthcare Pvt.Ltd. Wakad, pune
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Male and female subjects 30-60 years of age (both inclusive) 2.Subject diagnosed with cervical spondylitis with or without nerve compression for more than three months. 3.Pain in the neck and shoulder, and difficulty with neckline rotation, flexion, extension,etc. 4.Subject have Muscle spasm, Numbness, Tingling sensation, and joint stiffness. 5.Be willing to refrain from taking analgesics, anti-inflammatory agents, corticosteroids, muscle relaxants, etc. during the entire trial. 6.An ambulatory subject can provide verbal and written consent and is ready to comply with all study procedures.

Exclusion criteria

Exclusion criteria: 1. Patients suffering from a pathological condition like a Bone tumor, Tuberculosis spine, etc. 2. History of injury to the cervical spine with the major surgical intervention will be excluded. 3. Female subjects, who are pregnant, breastfeeding, or planning to become pregnant. 4. Patients who are unable to walk without support and/or confined to a wheelchair or bedridden. 5. History of psychiatric disorder that may impair the ability of subjects to provide written informed consent.

Design outcomes

Primary

MeasureTime frame
1. To study Panchakarma Essentials efficacy in reducing cervical spondylitis pain. 2. To study the patient’s relief from stiffness & other associated symptomsTimepoint: Seven Sessions in two weeks

Secondary

MeasureTime frame
1. To study improvement in the Cervical Range of Movement. 2. To assess the improvement in the Quality of life of a patientTimepoint: Seven Sessions in two weeks

Countries

India

Contacts

Public ContactDr Vaishnavi Patil

Mprex Healthcare Pvt. Ltd.

vaishnavi@mprex.in9834585994

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026