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Ayurveda Treatment Protocol of Varicose Veins

Validation of effectiveness of treatment principle and practice of combination therapy viz Sahachar Taila Paan Upanaha Basti Karma and Siravyadha in the management of Siraja Granthi varicose vein a clinical comparative study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101214
Enrollment
40
Registered
2026-01-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: I838- Varicose veins of lower extremities with other complications

Interventions

None listed

Sponsors

Pt Khushilal Sharma Government Autonomous Ayurveda College and Institute Bhopal 462003
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants aged between 18 and 65 years of either sex Participants presenting with the sign and symptom of varicose veins Participants willing to provide written informed consent either by themselves or through a legally acceptable representative LAR impartial witness in the case of illiterate subjects and who are willing to comply with all aspects of the study protocol

Exclusion criteria

Exclusion criteria: Patients already diagnosed with following conditions Varicose veins associated with Deep vein thrombosis Calcification Equinus deformity Valveless syndrome Patients who have undergone open venous surgeries such as Radio Frequency Ablation Thermal Ablation Patients with systemic illnesses including but not limited to Hypertension Diabetes mellitus Ischemic heart disease Anaemia Bleeding disorders Tuberculosis HIV Endocrine system related disorders with prolonged medication history Malignancy Any acute infection Patients with connective tissue disorders such as Systemic lupus erythematosus SLE Vasculitis Thrombophilia Patients on prolonged anticoagulant therapy Vulnerable groups including Pregnant women Lactating women mentally ill patients Patients unfit for Snehapana Bastikarma and Siravyadha Patients unwilling to provide written consent to participate in the study

Design outcomes

Primary

MeasureTime frame
Comparison of change in Venous Clinical Severity Score VCSS between the study groups from baseline to the end of treatmentTimepoint: 30 days

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr SHUBHAM SHUKLA

Pt Khushilal Sharma Government Autonomous Ayurveda College and Institute Bhopal 462003

salilujjain@gmail.com9425951126

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026