Radiofrequency Ablation vs Laser Ablation of the Incompetent Greater Saphenous Vein
Primary Purpose
Chronic Venous Insufficiency
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Ablation of the Incompetent Greater Saphenous Vein
ClosureFAST radiofrequency catheter
EVLT 980nm diode laser system
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Venous Insufficiency focused on measuring chronic venous insufficiency, varicose vein, greater saphenous vein
Eligibility Criteria
Inclusion Criteria:
- Patients with symptomatic chronic venous insufficiency.
- Patients in whom endovenous thermal ablation is clinically indicate.
- Have previously undergone at least 6 weeks of conservative treatment with compression stockings (unless they have venous ulcers, recurrent phlebitis, or bleeding varices).
- Have venous disease that meets CEAP clinical class 2 through 6.
- Have symptoms secondary to Greater Saphenous Vein insufficiency defined as reverse flow in the saphenous vein >0.5 seconds after calf compression or while standing.
Exclusion Criteria:
- Have previously undergone surgery, EVTA, or phlebectomy in that extremity (exclusive of spider vein injections or other cosmetic surface procedures).
- Have a history of DVT.
- Have a history of hypercoaguability disorder.
- Are pregnant or breastfeeding.
- Are nonambulatory.
Sites / Locations
- Virginia Commonwealth University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Radiofrequency Ablation
Laser Ablation
Arm Description
Device: ClosureFAST radiofrequency catheter (VNUS Medical Technologies Inc, San Jose, CA). Patients will have the intervention, ablation of the incompetent greater saphenous vein, using this device.
Device: EVLT 980nm diode laser system (Angiodynamics, Queensbury, NY). Patients will have the intervention, ablation of the incompetent greater saphenous vein, using this device.
Outcomes
Primary Outcome Measures
Percentage of Participants Without Recurrent Clinical Symptoms of an Incompetent Greater Saphenous Vein After Treatment.
Secondary Outcome Measures
Incidence Rate of Acute Complications
Number of acute complications at one and 6 weeks post intervention
Full Information
NCT ID
NCT02236338
First Posted
September 2, 2014
Last Updated
April 11, 2018
Sponsor
Virginia Commonwealth University
1. Study Identification
Unique Protocol Identification Number
NCT02236338
Brief Title
Radiofrequency Ablation vs Laser Ablation of the Incompetent Greater Saphenous Vein
Official Title
Radiofrequency Ablation vs Laser Ablation of the Incompetent Greater Saphenous Vein: A Prospective Randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
September 2008 (undefined)
Primary Completion Date
August 11, 2016 (Actual)
Study Completion Date
August 11, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Virginia Commonwealth University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this study is to perform a randomized, prospective trial comparing the two current methods of treatment for chronic venous insufficiency, in an effort to evaluate complications and outcomes for each method, and ultimately, to see if one is superior to the other.
Detailed Description
Chronic venous insufficiency (CVI) is estimated to affect 25 million Americans. This condition leads to varicose veins, aching, fatigue, swelling, ulcerations, and bleeding in the lower extremities. The most common cause is a refluxing or incompetent Greater Saphenous Vein (GSV). This condition results in pooling of deoxygenated blood in the lower extremities rather than successful transport of the blood back to the heart and lungs. The historical treatment has been to surgically remove or 'strip' the GSV so that blood is rerouted through the healthier deep veins. A less invasive treatment option, Endovenous Thermal Ablation, has emerged over the last decade and has virtually replaced stripping. This involves advancing a catheter under ultrasound guidance through the GSV and then advancing a laser fiber or radiofrequency probe through the catheter. These devices then produce the energy to destroy the vein as the catheters are slowly pulled back. While both radiofrequency ablation and laser ablation are accepted treatments, neither technology has been definitively proved to have fewer complications or superior results. This is in part because very few practices have the ability to make a head to head comparison between the two technologies and must choose one or the other secondary to financial constraints. The aim of this study is to perform a randomized prospective trial comparing the two modalities so that more definitive information to evaluate complications and outcome can be obtained and then recommendations on which, if either, technology is superior can be made.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Venous Insufficiency
Keywords
chronic venous insufficiency, varicose vein, greater saphenous vein
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Radiofrequency Ablation
Arm Type
Active Comparator
Arm Description
Device: ClosureFAST radiofrequency catheter (VNUS Medical Technologies Inc, San Jose, CA).
Patients will have the intervention, ablation of the incompetent greater saphenous vein, using this device.
Arm Title
Laser Ablation
Arm Type
Active Comparator
Arm Description
Device: EVLT 980nm diode laser system (Angiodynamics, Queensbury, NY).
Patients will have the intervention, ablation of the incompetent greater saphenous vein, using this device.
Intervention Type
Procedure
Intervention Name(s)
Ablation of the Incompetent Greater Saphenous Vein
Intervention Description
For each patient, the Greater Saphenous Vein (GSV) will be accessed just below the knee. After liberal use of anesthesia, the patient will undergo an ablation of the GSV. Half the patients will have this procedure performed using the Laser Ablation device and half will be treated using the Radiofrequency Ablation device. They will be randomly assigned to treatment.
Intervention Type
Device
Intervention Name(s)
ClosureFAST radiofrequency catheter
Intervention Type
Device
Intervention Name(s)
EVLT 980nm diode laser system
Primary Outcome Measure Information:
Title
Percentage of Participants Without Recurrent Clinical Symptoms of an Incompetent Greater Saphenous Vein After Treatment.
Time Frame
Annual follow up, up to 75 months
Secondary Outcome Measure Information:
Title
Incidence Rate of Acute Complications
Description
Number of acute complications at one and 6 weeks post intervention
Time Frame
up to 6 weeks post intervention
Other Pre-specified Outcome Measures:
Title
Incidence of Post-procedure Pain
Description
Measured with Visual Analog Scale (VAS), with a range of 1-10 with 10 being the most pain.
Time Frame
During post procedure recovery period in clinic, an expected average of 2 hours after surgery.
Title
Incidence of Objective Post-procedure Bruising
Description
Measured with bruising scale, with a range of 1-10 with 10 being the most bruising.
Time Frame
During post procedure recovery period in clinic, an expected average of 2 hours after surgery.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with symptomatic chronic venous insufficiency.
Patients in whom endovenous thermal ablation is clinically indicate.
Have previously undergone at least 6 weeks of conservative treatment with compression stockings (unless they have venous ulcers, recurrent phlebitis, or bleeding varices).
Have venous disease that meets CEAP clinical class 2 through 6.
Have symptoms secondary to Greater Saphenous Vein insufficiency defined as reverse flow in the saphenous vein >0.5 seconds after calf compression or while standing.
Exclusion Criteria:
Have previously undergone surgery, EVTA, or phlebectomy in that extremity (exclusive of spider vein injections or other cosmetic surface procedures).
Have a history of DVT.
Have a history of hypercoaguability disorder.
Are pregnant or breastfeeding.
Are nonambulatory.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Malcolm Sydnor, MD
Organizational Affiliation
Virginia Commonwealth University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Virginia Commonwealth University
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23298
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Radiofrequency Ablation vs Laser Ablation of the Incompetent Greater Saphenous Vein
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