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Panchakarma procedures in the management of Lumber Spondylosis

Comparative Efficacy Study of Baladiyapana Basti and Bala Taila Matra Basti in the Management of Katigraha w.s.r. to Lumbar Spondylosis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/03/024268
Enrollment
60
Registered
2020-03-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Intervention1: Bala Taila Matra Basti: Bala Taila Matra Basti will be administered in a dose of 60 ml every day through Rectal route as per the Standard Operating Procedure (SOP) of Anuvasna Basti of

Sponsors

National Institute of Ayurveda Jorawar Singh Gate Amber Road Jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients suffering from classical signs and symptoms of Katigraha w.s.r to Lumbar spondylosis. 2. Patients between 40 yrs to 60 yrs of age. 3. Male or female Patient willing and able to participate in the study for 16 days and follow up period of 15 days. 4. Patients able to provide informed consent. 5.Grade 2 and Grade 3 in X-ray findings through Lane Radiographic grading of lumbar disc degeneration on lateral views.

Exclusion criteria

Exclusion criteria: 1.Patients suffering from any acute diseases, infectious diseases, metabolic diseases, chronic diseases (like rheumatoid Arthritis, DM, Gout, TB, SLE, Ankylosing spondylitis etc) and other disease that may interfere with the course of treatment. 2. Patients suffering from Stenosis of spinal canal, Myelopathy (MRI optional), Lumbar carcinoma, spinal tumour or malignant tumours in any part of the body. 3. All type of Lumbar surgery or implanted instrumentation or prosthesis. 4. Patient having chronicity more than 5 yrs. 5. Pregnant women and lactating women are excluded.

Design outcomes

Primary

MeasureTime frame
The assessment of the clinical response by VAS (Visual Analogue Scale) and Oswestry disability index (ODI) scalesTimepoint: One Month

Secondary

MeasureTime frame
The assessment of the clinical response by Physical component scores (PCS) of SF-36Timepoint: One Month

Countries

India

Contacts

Public ContactSachin Sharma

National Institute of Ayurveda Jaipur

kshiprarajoria@gmail.com9001454100

Outcome results

None listed

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