The clinical study to evaluate effect of pre operative procedure in panchakrama in lumbar spondylosis

A comparative clinical study of siravedha with poorvakarma and siravedha without poorvakarma in gridhrasi W.S.R. sciatica - nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/066658

Enrollment

Registered

2024-05-02

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

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

Eligibility

Inclusion criteria

Inclusion criteria: patient diagnosed as gridhrasi based on clinical symptoms like pain radiating from kati to padanguli from posterior aspect of pad along with stambha ,toda ,spandana patient irrespective of gender, religion , economical status , education ,occupation etc. patient who are raktamokshan arha as per textual reference patient willing to gave consent for research purpose

Exclusion criteria

Exclusion criteria: patient below age of 30 yr and above age of 70 yr patient who are raktamokshan anarha as per textual reference patient suffering from haemolytic or any bleeding disorder patient having HB less than 9 gm% patient with any major systemic illness patient who will not give consent for research purpose

Design outcomes

Primary

Measure	Time frame
Decreasing visual analogue scale score Negative SLR testTimepoint: Duration of treatment 21 days	—

Secondary

Measure	Time frame
To assess efficacy of poorvakarma in siaravedha To stanadardize SOP of siravedhaTimepoint: Duration of treatment 21 days Follow up on 7th, 14th and 21st day	—

Countries

India

Contacts

Public ContactVd Shrutika Jayendra Bhand

MES Ayurved mahavidyalaya and research centre

vrushaliswami2009@gmail.com9422856123

Outcome results