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To Relieve Pain in Vataja Gridhrisi (Sciatica) with Nirgundi Taila Matra Vasti And Investigating Its Bioavailability

Effectiveness of Nirgundi Taila Matra Vasti in Alleviating Pain Associated With Vataja Gridhrisi (Sciatica) And Investigating Its Bioavailability: An Open-Labelled, Single Arm, Exploratory Clinical Trial. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088716
Enrollment
60
Registered
2025-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: G55- Nerve root and plexus compressionsin diseases classified elsewhere

Interventions

None listed

Sponsors

Dr Finbe Baby
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients presenting with clinical features of Gridhrasi (sciatica). 2 Gridhrasi (sciatica) patients with type 2 diabetes mellitus and hypercholestremia will be evaluated separately to see whether these diseases affect the efficacy and bio-availability of Nirgundi Taila Matra Vasti. 3 SLR test ranging between 310-700. 4 Patients willing to sign the consent form.

Exclusion criteria

Exclusion criteria: 1 Subjects of either sex having age below 18 years and above 60 years. 2 Patients having cardiac diseases, renal diseases, endocrine disorders and other systemic disorders. 3 Diagnosed cases of tuberculosis of spine, spinal tumors, vertebral fractures, surgical conditions, hyperuricaemia and autoimmune diseases like RA, ankylosing spondylitis. 4 Pregnant and lactating women. 5 Patient who had taken the Nirgundi in any form before starting the trial

Design outcomes

Primary

MeasureTime frame
1.To evaluate the efficacy of Nirgundi Taila Matra Vasti in alleviating pain associated with Vataja Gridhrasi (sciatica). 2.To assess the improvement in signs and symptoms of Vataja Gridhrasi (sciatica). Timepoint: 0 DAY, 7 DAY, 14 DAY

Secondary

MeasureTime frame
1. To assess the bio-availability of Nirgundi Taila when administered through rectal routeTimepoint: 0 DAY, 7 DAY, 14 DAY

Countries

India

Contacts

Public ContactDr Preetpal Singh

Glocal University

singhpreet523@gmail.com7015367776

Outcome results

None listed

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