A Study to find the most effective location for Siravedha treatment( A traditional ayurvedic procedure) Above and Below Knee Joint to relieve sciatica pain

Comparative Assessment of Anatomical site for Siravedha(Venepuncture) above and below knee joint in the management of Gridhrasi(Sciatica) Randomised Controlled Trial - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/12/078778

Enrollment

Registered

2024-12-30

Start date

Unknown

Completion date

Unknown

Last updated

2025-02-03

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

Conditions

Health Condition 1: M543- Sciatica

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients between 25-45 years of age, irrespective of gender, caste, and religion will be included. 2.Patients who had been pre-diagnosed with sciatica under lower back ache. 3. Subjects who are ready to give consent for trial with firm residential address and contact numbers.

Exclusion criteria

Exclusion criteria: 1.Patient with similar musculoskeletal conditions like sciatica but with other cause for lower back ache. 2.Patinets with other systemic disorders e.g. CAD, HTN, HIV, DM, TB, HBsAg, REACTIVE ETC. or any condition debilitating conditions. 3.Pregnant women and lactating mother. 4.Patients with Hb below 10 gm% and deranged bleeding and clotting time. 5. Patients diagnosed with specific diseases-spinal malignancies, spinal infection, inflammatory spondylitis and other malignancies 6. Gridhrasi due to traumatic injuries. 7. Gridhrasi developed due to any post-surgical complication 8. Gridhrasi associated with systemic/metabolic disorders. 9. Congenital deformity of vertebral column.

Design outcomes

Primary

Measure	Time frame
1.Assessment of preferred anatomical site for siravedha above and below knee joint. 2.Assess the more effective anatomical site for the siravedha.Timepoint: 14 days	—

Secondary

Measure	Time frame
1.Improvement in visual analogue scale for pain intensity 2.Improvement in Gradation of cardinal parametersTimepoint: 14 days	—

Countries

India

Contacts

Public ContactDr Rahul Ramkisan Phate

Ch Brahm Prakash Ayurved Charak Sansthan

rahulphate99@gmail.com7798705344

Outcome results