Skip to content

integrity approach for Venous Ulcer treatment.

Management of Venous Ulcer by Endovenous Laser Ablation, Four Layer Bandage and Leech Therapy-A Randomized Controlled Trial Study.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/050023
Enrollment
100
Registered
2023-02-23
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: L978- Non-pressure chronic ulcer of other part of lower leg

Interventions

None listed

Sponsors

Department of Shalya Tantra.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Any Patient irrespective of sex or religion falling between 18-60 years of age. known case of venous ulcers irrespective of duration.

Exclusion criteria

Exclusion criteria: Ulcers other than of venous ulcers. Malignancy. those allergic to local anesthetics. hyper coagulable condition. peripheral arterial insufficiency. lymphedema. poor general health/ Immuno- compromised state. recent thromboembolism. known type 2 DM. HIV/HbsAg/Anti HCV Positive

Design outcomes

Primary

MeasureTime frame
Assessment of venous ulcer would be done on the basis of: •Venous Clinical Severity Score (VCSS) •primary 12 questions of Aberdeen Venous Vein Questionnaire (AVVQ) •Duplex Ultrasonography (before and after 6 months of treatment) •VAS Score (Visual analog scale) •Wound measurement application (Measurement of Length, Width and Depth by wound measure application before, during and after treatment) •MMPs Timepoint: The assessment of ulcer and other symptoms of Chronic Venous Ulcer will be assessed after the completion of treatment, that is at 4 weeks.

Secondary

MeasureTime frame
The assessment of Venous ulcer would be done during follow-up- . To look for remission/progression of the disease. . To find out any recurrence and complication of venous ulcer. . Further recommendation for caution and treatment as required. Timepoint: secondary outcome will assessed at the period of 8 weeks.

Countries

India

Contacts

Public ContactDr Priyanka singh

Faculty of Ayurveda, IMS, BHU, Varanasi.

dr.arunbhu@gmail.com9451050860

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026