Skip to content

Use of Erandmooladi Niruha Basti and Erand Taila with Dashmoola Kwatha in Lumbar Spondylosis

A comparative study of Erandmooladi Niruha Basti and Erand Taila with Dashmoola Kwatha in tha management of Katishoola with special reference to Lumbar Spondylosis - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073237
Enrollment
60
Registered
2024-09-02
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: M470- Anterior spinal and vertebral artery compression syndromes

Interventions

None listed

Sponsors

Government P.G. Ayurveda College and Hospital Varanasi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex between 25 to 70 years of age. 2. Patients who have history of less than 1 year. 3. Patients who have the signs and symptoms of Katishoola and radiological early degenerative changes. 4. Patients who are willing to sign the consent for study participation. 5. Patients who are able and willing to complete the treatment schedule. 6. Patients who fit into the criteria for Bastikarma.

Exclusion criteria

Exclusion criteria: 1. Patients below the age of 25 years and above 70 years. 2. Patients who have Spinal Tumor, Tuberculosis of vertebral bodies, Malignant diseases of the pelvis. 3. Patients who recently had lumbar surgery or implanted instrumentation or prostheses. 4. Patients with chronic metabolic pathologies ie; Ankylosing Spondylosis, Rheumatoid Arthritis, Psoriatic Arthritis, Gouty Arthritis. 5. Patients having referred pain in the lower back such as in case of Renal Stones, Appendicitis, Pancreatitis, PID, Leucorrhea, Abdominal Aortic Aneurysm. 6. Pregnant and Lactating women. 7. Patients with any immunocompromised disease like AIDS, Tuberculosis etc. 8. Epilepsy or any other serious systemic illness. 9. Patients unwilling to participate in the trial. 10. Patients who do not fit into the criteria for Bastikarma.

Design outcomes

Primary

MeasureTime frame
Relief in pain, numbness and stiffnessTimepoint: 7 days

Secondary

MeasureTime frame
Complete relief in chief complaints of Lumbar SpondylosisTimepoint: 30 days

Countries

India

Contacts

Public ContactDr Jyoti Mishra

Government P.G. Ayurveda College and Hospital Varanasi

doctorjyotimisra@gmail.com9026310346

Outcome results

None listed

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