Clinical Evaluation of the Siravedh Device in the Management of Sira Granthi with a Focus on Varicose Veins

Development of siravedh device with clinical study to evaluate the effect of Siravedh with siravedh device in the management of Sira granthi with special reference to varicose vein - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/086927

Enrollment

Registered

2025-05-14

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

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

Conditions

Health Condition 1: I839- Asymptomatic varicose veins of lower extremities

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient presenting with symptopms of primary varicose veins in lowerlimb Such as tortuous dilated veins,pain,skin discololation,itching and oedema. 2. Age 18 to 60 of both the gender

Exclusion criteria

Exclusion criteria: 1.Varicose veins associated with deep vein thrombosis DVT and venous ulcer 2.Patient who have gone under open venous surgery 3.Patient with known bleeding disorders, anemia, uncontrolled diabetes, and sever systemic disorders 4.Patient ayogya for siravedh.as per sushruta 5.Patient with old age , kids, pregnant lady

Design outcomes

Primary

Measure	Time frame
To design and develop Siravedh DeviceTimepoint: 3 months	—

Secondary

Measure	Time frame
To evaluate the efficacy of Siravedh with the help of siravedh device in management of Sira granthi.Timepoint: Assessment will be done on baseline, 1st week, 2nd week, 3rd week & 4th week.	—

Countries

India

Contacts

Public ContactDr Chandrakant Pawar

Parul Institute of Ayurved and Research

drchandrakantpawar@gmail.com9822711566

Outcome results