In this study 1 group will be receive nirgundi patra pinda sweda and 2nd group will be receive nirgundi taila katibasti.

A comparative clinical study of nirgundi patra pinda sweda and nirgundi taila katibasti in the management of gridhrasi - NIL

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/09/073848

Enrollment

Registered

2024-09-12

Start date

Unknown

Completion date

Unknown

Last updated

2024-09-16

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

Conditions

Health Condition 1: M488- Other specified spondylopathies

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients with classical symptoms of gridhrasi Both gender will be selected Snehana arha Swedana arha Age group- 20 to 60 yrs Patients with positive SLRT

Exclusion criteria

Exclusion criteria: fracture related to LS of spine pregnant women spinal tuberculosis any systemic conditions which may interfere the treatment.

Design outcomes

Primary

Measure	Time frame
To compare the effect of nirgundi patra pinda sweda and nirgundi taila katibasti in Gridhrasi.Timepoint: Treatment will be given for 7 days patients will be assessed on oth, 7th day and follow up on 15th day.	—

Secondary

Measure	Time frame
To assess the effect of nirgundi patra pinda sweda in gridhrasi To assess the effect of nirgundi taila katibasti in gridhrasi.Timepoint: Patients will be assessed on 0th , 7th day & follow up on 15th day.	—

Countries

India

Contacts

Public Contactdr Bhagyashri Ashok Kale

Sumatibhai shah ayurveda mahavidyalay pune

drpriyankakeram@gmail.com8485022857

Outcome results