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Efficacy of Agnikarma and Katibasthi with Devadaru Baladi Taila in the Management of lumbar spondylosis

Efficacy of Agnikarma and Katibasthi with Devadaru Baladi Taila in the Management of Katisandhigata Vata (lumbar spondylosis) An Open Labelled Randomised Comparative Clinical Trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085512
Enrollment
40
Registered
2025-04-24
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Institute of Teaching and Research in Ayurveda,Jamnagar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients between age group 30-70 years of either gender. 2.Patient suffering from pain, stiffness, numbness irrespective to demographic data. 3.X-ray investigation with reduction in intervertebral disc space, loss of lordosis and presence of lumbar scoliosis taken for the study. 4.Patients who are of niramaja condition included.

Exclusion criteria

Exclusion criteria: 1.Patients below 30 years and above 70 years. 2.Patients of uncontrolled diabetes mellitus (RBS above 150mg/dl), R.A. (Rheumatoid arthritis) positive, hypertension. 3.Other diseases like paralysis, Parkinson s disease, severe anaemia, cardiac diseases, renal diseases and endocrine diseases, severe anaemia and Malignancy. 4.Pregnant/lactating female. 5.Agnikarma Ayogya patients as per classics i.e. Pitta Prakruti diseased with Rakta-Pitta, Atisara, Durbala, Bheeru, Vranita, Aswedya and those having srotorodha, balabramsha. 6.Other diseases like sacroiliac joint arthritis, lymphomas, pelvic malignancy, etc., patients will be excluded. 7.Patients suffering from trauma,fracture, systemic diseases, Sciatica with neurological damage, contraindications to Agnikarma such as patients affected with multiple wounds, sciatica with SLR test positive less than 30 and more than 70 .

Design outcomes

Primary

MeasureTime frame
Relief in pain stiffness numbness over lumbar region Timepoint: 1st day 7th day 14th day 21st day 28th day

Secondary

MeasureTime frame
Absence of recurrence in followup period.Timepoint: 60 days

Countries

India

Contacts

Public ContactProf Dr T S Dudhamal

Institute of Teaching and Research in Ayurveda, Jamnagar

drtsdudhamal@gmail.com9428671939

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026