A clinical study to see the effectiveness of yashtyahvyadi ksheer basti for 9day in the management of vatarakta(Gout)

Effectiveness of an open label single arm study with yashtyahvyadi ksheer basti as modified kala basti in vatarakta(Gout) - NILL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/070269

Enrollment

Registered

2024-07-09

Start date

Unknown

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

Health Condition 1: M109- Gout, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient fulfilling the diagnostic criteria 2.Patient of either gender,from the age group of 18 to 60 3.Increased serum uric acid level (more than 7mg/dl in male and more than 6mg/dl in female 4.Fit for basti karma 5.Willing to sign the consent form

Exclusion criteria

Exclusion criteria: 1.Patient having history of other systemic diseases 2.Pateint with joint deformity and fractures 3.History of renal failure,HIV,HBsAg, Tuberculosis, Carcinoma 4.Congenital bone deformity 5.Pregnant and lactating women

Design outcomes

Primary

Measure	Time frame
Signs and Symptoms of Vatarakta(Gout)will be assessed by giving suitable scoring after 9th day of basti and 18th day of follow up with kaishore guggulu 500mg BD(after food with lukewarm water) The disease activity of the patient will be, assessed by Likert scale,Range of movement measured with Goniometer and serum uric acid levelTimepoint: 18 day	—

Secondary

Measure	Time frame
NoneTimepoint: None	—

Countries

India

Contacts

Public ContactDr Lohith B A

Sri Dharmasthala Manjunatheshwara College of Ayurveda and Hospital

drlohithba@sdmcahhassan.org9886749168

Outcome results