Clinical trial
RCT Comparing Standard Cannula Delivered FS, UGFS and ClariVein® in the…
NCT02010437 · Hull University Teaching Hospitals NHS Trust, Other · Withdrawn
Key facts
| NCT number | NCT02010437 |
|---|---|
| Title | RCT Comparing Standard Cannula Delivered FS, UGFS and ClariVein® in the Management of SVI |
| Official title | A Randomised Clinical Trial Comparing Standard Cannula Delivered Foam Sclerotherapy, Catheter Directed Foam Sclerotherapy and ClariVein® Mechanochemical Ablation in the Management of Superficial Venous Insufficiency. |
| Acronym | EVCA |
| Lead sponsor | Hull University Teaching Hospitals NHS Trust, Other |
| Status | Withdrawn |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | Superficial Venous Insufficiency, Varicose Veins |
| Intervention type | Drug |
| Interventions | Sodium Tetradecyl Sulphate (STS) |
| Enrollment | 0 |
| Start date | Jan 1, 2014 |
| Primary completion | Jan 1, 2015 |
| Completion | Apr 1, 2015 |
| First posted | Dec 12, 2013 |
| Last update posted | Jul 15, 2019 |
| Countries | United Kingdom |
At a glance
- 1–9 Study sites
- No Results posted
- 1–9 Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: