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NCT02236338 · ClinicalTrials.gov registry record · Phase 4
Radiofrequency Ablation vs Laser Ablation of the Incompetent Greater Saphenous Vein
A Phase 4 study of Chronic Venous Insufficiency, sponsored by Virginia Commonwealth University.
- Completed
- Registry status
- Phase 4
- Development phase
- 200
- Enrollment target
- 1
- Study location
NCT02236338 is a Phase 4 study of Chronic Venous Insufficiency that has completed, run by Virginia Commonwealth University. The registered enrollment target is 200 participants, above the 110-participant average among 3 other Chronic Venous Insufficiency trials with a reported enrollment target (82% higher). The trial reports 1 study location across 1 state.
The verdict
NCT02236338, a Phase 4 study of Chronic Venous Insufficiency, has completed, sponsored by Virginia Commonwealth University.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 200 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- PROCEDURE Ablation of the Incompetent Greater Saphenous Vein
- DEVICE ClosureFAST radiofrequency catheter
- DEVICE EVLT 980nm diode laser system
Study Locations (1)
Virginia
- Virginia Commonwealth University - Richmond
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2008-09 |
| Est. Completion | 2016-08-11 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02236338
The ClinicalTrials.gov registry entry for NCT02236338 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 110-participant average among 3 other Chronic Venous Insufficiency trials with a reported enrollment target (82% higher). The listed sponsor is Virginia Commonwealth University, which has 558 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Chronic Venous Insufficiency appearing as the primary indexed condition, and to 3 interventions - of which Ablation of the Incompetent Greater Saphenous Vein is the first listed.
NCT02236338 reports 1 study location spanning 1 distinct geographic area - top geographies include Virginia.
Frequently Asked Questions
What is clinical trial NCT02236338 about?
NCT02236338 is a clinical study titled "Radiofrequency Ablation vs Laser Ablation of the Incompetent Greater Saphenous Vein". 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.
What is the current status of trial NCT02236338?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 200 participants. The study started on 2008-09. Estimated completion is 2016-08-11.
What conditions does trial NCT02236338 study?
This clinical trial studies the following conditions: Chronic Venous Insufficiency.
What interventions are being tested in trial NCT02236338?
The interventions under investigation include: Ablation of the Incompetent Greater Saphenous Vein (PROCEDURE), ClosureFAST radiofrequency catheter (DEVICE), EVLT 980nm diode laser system (DEVICE).
Who is sponsoring clinical trial NCT02236338?
This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02236338 being conducted?
This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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