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To evaluate the effect of Kati Basti and Matra Basti in Katigraha wsr to Lumbar Spondylosis

A Comparative Clinical Study to evaluate the efficacy of Kati Basti and Matra Basti with Shairiya Tail along with Oral Administration of Abhadya Churna in cases of Katigraha wsr to Lumbar Spondylosis - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084111
Enrollment
60
Registered
2025-04-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: M478- Other spondylosis

Interventions

None listed

Sponsors

State Ayurvedic College And Hospital, Lucknow
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients will be selected between 25-65 yrs of age irrespective of sex, caste, religion. All socio-economic people. Patient voluntarily willing to sign the consent form for the clinical trial. Patients of pain and stiffness in lumbar region with or without non-essential criteria along with positive radiological findings of Lumbar Spondylosis.

Exclusion criteria

Exclusion criteria: Patient not from the age group mentioned in the inclusion criteria. In pregnant and lactating women. Patients having complication of Lumbar Spondylosis like spinal tuberculosis, space occupying lesion, prolapsed disc, vertebral fracture & Spondylolisthesis, Ankylosing Spondylitis, Radiculopathy etc. Patients with diagnosed case of cardiac disease, renal disease & other systemic disorders. Patient having structural deformity likes lordosis or any spinal curvature. Patient having past history of rheumatoid or rheumatic arthritis, pot s spine etc. Patient having other pathology like pelvic inflammatory diseases etc. Patient where steroids dependent.

Design outcomes

Primary

MeasureTime frame
Kati shoola(Pain in lumbar region). Kati Stambha/Kati Graha (Stiffness in Lumbar region) Timepoint: Before Trial 15th day,30th day, 45th day, 60th day, After Trial

Secondary

MeasureTime frame
Restricted movement on flexion and extension Tenderness in Lumbar region Numbness in lower part of the body Prickling sensation in the lower part of the body Timepoint: Before Trial 15th day,30th day, 45th day, 60th day, After Trial

Countries

India

Contacts

Public ContactVaishnavi Lohiya

State Ayurvedic College and Hospital Lucknow

drshachi09@gmail.com9415063998

Outcome results

None listed

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