Medtronic Endovascular
Medtronic Endovascular sponsors 25 registered US clinical trials on ClinicalTrials.gov, 2 of them currently recruiting, and 18 completed. 2 of these trials are in Phase 3-4 (later-stage) and 0 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Great Saphenous Vein (GSV) With Venous Reflux Disease, with 2 trials.
Trial Pipeline
25 total, page 1 of 1
Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectomy System
NCT07335341
Onyx™ Liquid Embolic IDE Clinical Study
NCT06742801
Ellipsys Vascular Access System Post Market Surveillance (PS) Study
NCT04484220
VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial
NCT03820947
FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease and Critical Limb Ischemia
NCT04120610
CAPERE Thrombectomy System Post-Market Clinical Follow Up Study
NCT03869645
ABRE Clinical Study of the Abre Venous Self-expanding Stent System
NCT03038438
IN.PACT™ AV Access IDE Study
NCT03041467
VeClose Five Year Follow-Up Extension Study
NCT03455699
Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD
NCT02363972
VenaSeal Sapheon Closure System Pivotal Study (VeClose)
NCT01807585
EverFlex Post Approval Study
NCT01680835
IN.PACT Admiral Drug-Coated Balloon vs. Standard Balloon Angioplasty for the Treatment of Superficial Femoral Artery (SFA) and Proximal Popliteal Artery (PPA)
NCT01566461
DURABILITY™ Iliac Study
NCT01400919
VISIBILITY™ Iliac Study
NCT01402700
Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study
NCT01341483
RFS (Radiofrequency Stylet) - Radiofrequency Perforator Vein Treatment Study
NCT01079598
Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE)
NCT00880230
The Complete® SE SFA Study for the Treatment of SFA/PPA Lesions
NCT00814970
The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of Iliac Vessel Disease) Study
NCT00753337
The Complete® Self-Expanding Stent and Stent Delivery System Registry
NCT00730730
Proximal Protection With The Mo.Ma Device During Carotid Stenting
NCT00744523
Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval Study
NCT00530504
ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter, Single-Blinded, Randomized Study.
NCT00509392
Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial
NCT00619775
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 3 | 1 |
| Phase 4 | 1 |
Therapeutic Areas
What the Pipeline for Medtronic Endovascular Shows
According to the ClinicalTrials.gov registry, Medtronic Endovascular is linked to 25 US clinical trials across every stage of research activity. Of those, 2 studies are currently recruiting, about 8% of the sponsor's indexed portfolio, and 18 are already marked complete, representing roughly 72% of the total.
The phase mix for Medtronic Endovascular reports 2 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Medtronic Endovascular is Great Saphenous Vein (GSV) With Venous Reflux Disease with 2 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.