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A study to know the Efficacy of Patrapinda Sweda in the management of katigraha(lumbar spondylosis)

To Study The Efficacy Of Patrapinda Sweda In The Management Of Katigraha (Lumbar Spondylosis)-A Controlled Clinical Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072565
Enrollment
40
Registered
2024-08-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: M479- Spondylosis, unspecified

Interventions

None listed

Sponsors

Dr Poojashree NK
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients of either gender and of age between 30 – 50 years 2 Fulfilling the diagnostic criteria with the presentation of signs and symptoms of katigraha 3 Radiologically early degenerative changes 4 Patients suitable for the Swedana procedure 5 Patients who are voluntarily willing to sign informed consent.

Exclusion criteria

Exclusion criteria: 1 Patients having spinal tumor, malignant diseases of the pelvis, tuberculosis of vertebral bodies 2 Lumbar region surgery or implanted instrumentation 3 Chronic metabolic pathologies like ankylosing spondylosis, rheumatoid arthritis, psoriatic arthritis, gouty arthritis, pelvic inflammatory disease, and infective arthritis 4 Pregnancy 5 Patients with major systemic disorders that may interfere with the course of treatment

Design outcomes

Primary

MeasureTime frame
1. Significant Reduction in Pain measured using VAS scale 2. Significant Reduction in stiffness assessed through Gradings 3. Significant Improvement in Range of movements (Schober’s test)Timepoint: 1st assessment 0th day (Before treatment) 2nd assessment 8th day (after treatment)

Secondary

MeasureTime frame
Improved Quality of life-related to the lumbar spine by reducing the pain, and dependency & improving functionality through the Oswestry disability index (questionaries method)Timepoint: 1st assessment 0th day (Before treatment) 2nd assessment 8th day (after treatment)

Countries

India

Contacts

Public ContactDr Arun B Jainer

Shri Dharmasthala Manjunatheshwara Institute of Ayurveda and Hospital Bengaluru

draruns@gmail.com8660732371

Outcome results

None listed

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