Medtronic Endovascular

25 total trials 2 currently recruiting 18 completed

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

RECRUITING

Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectomy System

NCT07335341

RECRUITING NA

Onyx™ Liquid Embolic IDE Clinical Study

NCT06742801

COMPLETED NA

Ellipsys Vascular Access System Post Market Surveillance (PS) Study

NCT04484220

TERMINATED NA

VenaSeal Spectrum: Global Post-Market Randomized Controlled Trial

NCT03820947

TERMINATED

FlowMet-R Blood Flow Measurement for the Diagnosis of Peripheral Artery Disease and Critical Limb Ischemia

NCT04120610

TERMINATED

CAPERE Thrombectomy System Post-Market Clinical Follow Up Study

NCT03869645

COMPLETED NA

ABRE Clinical Study of the Abre Venous Self-expanding Stent System

NCT03038438

COMPLETED NA

IN.PACT™ AV Access IDE Study

NCT03041467

COMPLETED

VeClose Five Year Follow-Up Extension Study

NCT03455699

COMPLETED NA

Percutaneous Less Invasive AV Fistula for Vascular Access in ESRD

NCT02363972

COMPLETED NA

VenaSeal Sapheon Closure System Pivotal Study (VeClose)

NCT01807585

COMPLETED NA

EverFlex Post Approval Study

NCT01680835

COMPLETED NA

IN.PACT Admiral Drug-Coated Balloon vs. Standard Balloon Angioplasty for the Treatment of Superficial Femoral Artery (SFA) and Proximal Popliteal Artery (PPA)

NCT01566461

COMPLETED NA

DURABILITY™ Iliac Study

NCT01400919

COMPLETED NA

VISIBILITY™ Iliac Study

NCT01402700

TERMINATED

Incidence of Male Pudendal Artery Stenosis in Suboptimal Erections Study

NCT01341483

TERMINATED NA

RFS (Radiofrequency Stylet) - Radiofrequency Perforator Vein Treatment Study

NCT01079598

COMPLETED NA

Iliac Artery Treatment With The Invatec Scuba™ Cobalt Chromium Stent (INTENSE)

NCT00880230

COMPLETED NA

The Complete® SE SFA Study for the Treatment of SFA/PPA Lesions

NCT00814970

COMPLETED NA

The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of Iliac Vessel Disease) Study

NCT00753337

COMPLETED NA

The Complete® Self-Expanding Stent and Stent Delivery System Registry

NCT00730730

COMPLETED NA

Proximal Protection With The Mo.Ma Device During Carotid Stenting

NCT00744523

COMPLETED NA

Carotid Revascularization With ev3 Arterial Technology Evolution Post Approval Study

NCT00530504

COMPLETED Phase 4

ClosureFAST vs. Laser Ablation for the Treatment of GSV Disease: A Multicenter, Single-Blinded, Randomized Study.

NCT00509392

COMPLETED Phase 3

Carotid Revascularization With ev3 Arterial Technology Evolution (CREATE) Trial

NCT00619775

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.