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Radiofrequency Ablation vs Laser Ablation of the Incompetent Greater Saphenous Vein
NCT02236338 · View on ClinicalTrials.gov ↗
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. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Virginia Commonwealth University, which has 513 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT02236338 reports 1 study location spanning 1 distinct geographic area — top geographies include Virginia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
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). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02236338?
This trial is sponsored by Virginia Commonwealth University, which has 513 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
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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