Medtronic

30 total trials 3 currently recruiting 19 completed

Medtronic sponsors 30 registered US clinical trials on ClinicalTrials.gov, 3 of them currently recruiting, and 19 completed. The most-studied condition in this pipeline is Bradycardia, with 6 trials.

Trial Pipeline

30 total, page 1 of 1

RECRUITING

Post Market Evaluation of Real World Outcomes and Durability to Support Implantable Inceptiv™ Spinal Cord Stimulation Therapy

NCT07507422

RECRUITING

Product Surveillance Registry

NCT01524276

RECRUITING

Product Performance Report: Evaluate Long-term Reliability & Performance of Medtronic Marketed Cardiac Therapy Products

NCT00271180

ACTIVE NOT RECRUITING

Enlighten Study: The EV-ICD Post Approval Registry

NCT06048731

ACTIVE NOT RECRUITING

IN.PACT™ AV Access Post-Approval Study (PAS002)

NCT04543539

ACTIVE NOT RECRUITING

Personalized Therapy Study - Intrinsic Antitachycardia Pacing Post-Approval Study (iATP PAS)

NCT04496518

ACTIVE NOT RECRUITING

Personalized Therapy Study - HFRS (TriageHF) Post Approval Study

NCT04489225

ACTIVE NOT RECRUITING

Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pacemakers (Micra AV CED)

NCT04235491

ACTIVE NOT RECRUITING

Personalized Therapy Study - Attain Stability Quad Post-Approval Study

NCT04024943

ACTIVE NOT RECRUITING

Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemakers

NCT03039712

ACTIVE NOT RECRUITING

Micra Transcatheter Pacing System Post-Approval Registry

NCT02536118

COMPLETED

Medtronic Signia SDR Product Surveillance Registry

NCT05095935

COMPLETED

Micra AV Transcatheter Pacing System Post-Approval Registry

NCT04253184

COMPLETED

Personalized CRT - MPP Post Approval Study

NCT03232944

COMPLETED

3T MRI CIED Post-Approval Study

NCT02969395

COMPLETED NA

Micra Transcatheter Pacing System Continued Access Study Protocol

NCT02488681

COMPLETED

Attain Performa™ Left Ventricular (LV) Quadripolar Leads Chronic Performance Study

NCT02294331

COMPLETED

The Product Surveillance Registry REVERSE Post Approval Study

NCT01660035

COMPLETED

Personalized CRT - PSR

NCT03723265

COMPLETED

DF4 Connector System Post-Approval Study

NCT01638897

COMPLETED

Model 4396 Left Ventricular (LV) Lead Chronic Performance Study

NCT01361685

COMPLETED

Model 4296 Left Ventricular (LV) Lead Chronic Performance Study

NCT01361672

COMPLETED

SureScan Post-Approval Study

NCT01299675

COMPLETED

Model 4196 Left Ventricular (LV) Lead Chronic Performance Study

NCT00930904

COMPLETED

Model 4195 Left Ventricular (LV) Lead Chronic Performance Study

NCT00869921

COMPLETED

MEDTRONIC ADAPTA, VERSA AND SENSIA nEw3 POST APPROVAL STUDY

NCT01076374

COMPLETED NA

Platelets for Acute Wound Healing

NCT00125086

COMPLETED NA

Platelets in Acute Wounds: A Pilot Study (PAWS)

NCT00199992

COMPLETED

Model 4968 CAPTURE EPI® STERIOD-ELUTING BIPOLAR EPICARDIAL PACING LEAD Post-approval Study

NCT01076361

COMPLETED

Model 4965 Post-Approval Study

NCT01076348

What the Pipeline for Medtronic Shows

According to the ClinicalTrials.gov registry, Medtronic is linked to 30 US clinical trials across every stage of research activity. Of those, 3 studies are currently recruiting, about 10% of the sponsor's indexed portfolio, and 19 are already marked complete, representing roughly 63% of the total.

The phase mix for Medtronic reports 0 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 is Bradycardia with 6 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.