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The Role of Advanced Therapies in Spinal Health: A Comparison of Vacuum IFT, Cryotherapy, Tecar Therapy, and Laser Therapy

To study the Clinical outcomes of Vacuum IFT,Cryotherapy,Tecar or Laser Therapy combinations on patients with Spinal Ailments - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080358
Enrollment
150
Registered
2025-02-12
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: M638- Disorders of muscle in diseases classified elsewhere

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Stavya Spine Hospital and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age 18-95 years. 2.Male and Female patients. 3.Pain duration greater than 3 months. 4.NPRS score greater or equal to 3. 5.Diagnosed with: Postural problems Postural low back pain (LBP) Postural neck pain Trapezius muscle spasm Paraspinal muscle spasm Dorsal spine pain 6.Diagnosed by medical doctors or orthopaedic/spine surgeons. 7.Occupational spine ailments included. 8.Multivitamins permitted. 9.Willingness to participate and comply with the study protocol

Exclusion criteria

Exclusion criteria: 1. Neuropathic pain due to nerve root compression. 2. Diabetes mellitus. 3. Severe comorbidity 4. History of acute trauma or fracture. 5. Implanted pacemakers. 6. Pregnancy. 7. History of malignancy or infection. 8. Systemic musculoskeletal disease. 9. Epilepsy. 10. Recent Spinal surgery (within the last 6 months) 11. Psychiatric disorders. 12. Neurodegenerative diseases. 13. Deep Vein Thrombosis (DVT). 14. Tuberculosis. 15. Spinal instability or deformities (PIVD, lumbar canal stenosis, scoliosis, cervical canal ste-nosis, lysis). 16.Diabetic neuropathy. 17. Osteoporosis. 18. Current use of NSAIDs or muscle relaxants.

Design outcomes

Primary

MeasureTime frame
Pain Assessment: - Visual Analogue Scale (VAS) - Numeric Pain Rating Scale (NPRS) Disability and Functional Assessment: - Modified Oswestry Disability Index (ODI) - Roland Morris Disability Questionnaire - Neck Disability Index (NDI) Range of Motion (ROM): - Lumbar flexion and extension - Neck flexion and extension Quality of Life Assessment: - SF-36 Health Survey - Socioeconomic status via Kuppuswamy scale Timepoint: This is a prospective study involves a 3 4-week treatment phase and a 1 2-month follow-up period, requiring patient visits for data collection.—

Secondary

MeasureTime frame
NATimepoint: NA—

Countries

India

Contacts

Public ContactDr Akruti Dave

Stavya Spine Hospital and Research Institute

akruti@stavyaspine.com9512829717

Outcome results

None listed

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