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A Clinical Study on Static and Increment Dosage Patterns of Lashuna Rasayana in Gridhrasi w.s.r Sciatica

An Open Randomized Controlled Clinical Study on Static and Increment Dosage Patterns of Lashuna Rasayana in Gridhrasi w.s.r Sciatica

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/054080
Enrollment
370
Registered
2023-06-19
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: M511- Thoracic, thoracolumbar and lumbosacral intervertebral disc disorders with radiculopathy

Interventions

None listed

Sponsors

Dr Anupama S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of Gridhrasi/Sciatica between the age of 16 to 70 years. 2.Patients with radiological evidence of Lumbar Spondylosis. 3.Patients with radiological evidence of Disc Prolapse.

Exclusion criteria

Exclusion criteria: 1.Sciatica with Congenital deformities of spine 2.Neoplastic conditions of the spine with radicular pain. 3.Infections of the spine with Sciatica. 4.Patients with evidence of severe unstable renal, hepatic, hemopoitic and cardiac disorder as revealed by history and/or investigations which would decline the general condition of the patient and interfere with the present clinical trial. 5.Those with history of having received any investigational drug in the previous one month. 6.Patients taking antipyretics, analgesics, tranquilizers, hypnotics, excessive alcohol or any other drug which would interfere with the pain perception.

Design outcomes

Primary

MeasureTime frame
1.Change from baseline in Visual analogue scale for back pain intensity (katishula) 2.Change from baseline in Visual analogue scale for leg pain intensity (sakthishula) 3.Change from baseline in Visual analogue scale for leg stiffness intensity (stambha) [range 0 (better) -10 (worse); Time Frame: baseline, 18 days] 4.Change from baseline in the average angle of restriction while testing straight leg raising (saktiutkshep nigraha) [if unilateral the actual degree of restriction is noted, if bilateral average degree of restriction is considered; Time Frame: baseline, 18 days] 5.Change from baseline in Aberdeen back pain scale [Minimum back pain severity scale is 0, and maximum is 100%, The higher the score the greater the severity of the back pain; Time Frame: baseline, 18 days]Timepoint: 0, 18 days

Secondary

MeasureTime frame
1. Change from baseline in Oswestry Disability Index [minimum score 0 %, maximum 100%; 0% equals no disability, and 100% is the maximum disability possible; Time Frame: baseline, 18 days] 2. Change from baseline in Neurological Impairment Scale as per Herron & Turners Rating [Time Frame: baseline, 18 days] 3. Change from baseline in Sugar baker & Barofsky Clinical Mobility Scale [Time Frame: baseline, 18 days] 4. Change from baseline in Oswestry Disability Assessment Questionnaire [Time Frame: baseline, 18 days] Timepoint: baseline, 18 days

Countries

India

Contacts

Public ContactDr Anupama S

Parul Institute of Ayurveda Parul University

sangeeta.toshikhane26791@paruluniversity.ac.in9964596479

Outcome results

None listed

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