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NCT01458795 Clinical Trial

The Fate Of Calf Perforators After Endovenous Laser Ablation Of Saphenous Veins

Venous Insufficiency Clinical Trial

Official title:
The Fate Of Calf Perforators After Endovenous Laser Ablation Of Saphenous Veins

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01458795
Other study ID # bask 012
Secondary ID
Status Completed
Phase Phase 4
First received October 20, 2011
Last updated November 2, 2011

Study information
Verified date November 2011
Source Baskent University
Contact n/a
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the morphologic and hemodynamic changes in the calf perforators after endovenous laser ablation of saphenous veins.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Symptomatic patients who undergo EVLA procedure for saphenous vein insufficiency

Exclusion Criteria:

- Patients with a history of deep venous thrombosis (DVT)

- Previous varicose vein surgery or injection sclerotherapy

- Patients without superficial venous incompetency

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• Endovenous laser ablation

Locations
Country Name City State
Turkey Baskent University Adana

Sponsors (1)
Lead Sponsor Collaborator
Baskent University

Country where clinical trial is conducted

Turkey, 

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