Abbott Medical Devices

261 total trials 23 currently recruiting 186 completed

Abbott Medical Devices sponsors 261 registered US clinical trials on ClinicalTrials.gov, 23 of them currently recruiting, and 186 completed. 17 of these trials are in Phase 3-4 (later-stage) and 5 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Heart Failure, with 15 trials.

Trial Pipeline

261 total, page 4 of 6

COMPLETED

Trifecta™ Long Term Follow-Up (LTFU) Study

NCT01593917

COMPLETED

Thoratec's Reduce Driveline Trauma Through Stabilization and Exit Site Management Study

NCT01485666

COMPLETED

Driveline Silicone Skin Interface Registry

NCT01577433

COMPLETED NA

Safety and Efficacy of the Accent Magnetic Resonance Imaging™ (MRI) Pacemaker and Tendril MRI™ Lead

NCT01576016

COMPLETED

Quadripolar Pacing Post Approval Study

NCT01555619

COMPLETED NA

Post-Approval Study Protocol of the St. Jude Medical Trifecta Valve

NCT01514162

COMPLETED Phase 1

Traumatic Brain Injury Peripheral Nerve Study

NCT01588691

COMPLETED

Study of Reduced Anti-coagulation/Anti-platelet Therapy in Patients With the HeartMate II Left Ventricular Assist System (LVAS) (TRACE)

NCT01477528

COMPLETED NA

Therapy™ Cool Flex™ Irrigated Ablation System for Typical Atrial Flutter

NCT01408485

COMPLETED

Risk Assessment and Comparative Effectiveness of Left Ventricular Assist Device (LVAD) and Medical Management

NCT01452802

COMPLETED NA

Absolute Pro® MOMENTUM™

NCT01444378

COMPLETED Phase 3

Atrial Flutter Ablation With Contact Therapy Cool Path Ablation System Along With EnSite Velocity Contact System

NCT01401361

COMPLETED NA

Carotid Artery Stenting Outcomes in the Standard Risk Population for Carotid Endarterectomy

NCT01445613

COMPLETED NA

EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Eluting Coronary Stent Coronary Stents, Performance, and Technique in Chronic Total Occlusions

NCT01435031

TERMINATED NA

ST Monitoring to Detect Acute Coronary Syndrome Events in Implantable Cardioverter Defibrillator Patients

NCT01424722

COMPLETED NA

TactiCath Contact Force Ablation Catheter Study for Atrial Fibrillation

NCT01278953

COMPLETED

XIENCE V Everolimus Eluting Coronary Stent System (EECSS) China: Post-Approval, Single-Arm Study

NCT01249027

COMPLETED

Angio-Seal Interventional Radiology (IR) Registry

NCT01222104

COMPLETED

EXCEL Clinical Trial (Universal Registry)

NCT01205789

COMPLETED NA

EXCEL Clinical Trial

NCT01205776

COMPLETED

QuickFlex Micro Left Ventricular Lead Post Approval Study

NCT01179477

COMPLETED

A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter in Stenotic Lesions

NCT01186198

COMPLETED NA

Real Time 3-Dimensional Echocardiography for Left Ventricular Lead Site Selection to Reduce Cardiac Resynchronization Therapy Non-Responder Rates

NCT01278030

COMPLETED NA

FAME II - Fractional Flow Reserve (FFR) Guided Percutaneous Coronary Intervention (PCI) Plus Optimal Medical Treatment (OMT) Verses OMT

NCT01132495

COMPLETED NA

Evaluate the Safety and Efficacy of OAS in Treating Severely Calcified Coronary Lesions

NCT01092416

COMPLETED NA

AMPLATZER Cardiac Plug Clinical Trial

NCT01118299

COMPLETED NA

Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy

NCT01121107

COMPLETED

Risk Stratification and Benefits With Cardiac Resynchronization Therapy (CRT)

NCT00996086

COMPLETED NA

Irrigated Ablation System Evaluation for Atrial Fibrillation (AF)

NCT01056328

COMPLETED Phase 3

Clinical Evaluation of Therapy™ Cool Path™ Duo Cardiac Ablation System for the Treatment of Typical Atrial Flutter (AFL)

NCT00984204

COMPLETED NA

CentriMag RVAS U.S. Post-approval Study Protocol

NCT01568424

COMPLETED NA

Promote Q Cardiac Resynchronization Therapy Defibrillator (CRT-D) and Quartet Left Ventricular Heart Lead Study

NCT00990665

COMPLETED Phase 4

XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort

NCT01106534

COMPLETED NA

Comparison of the SUpera® PERipheral System in the Superficial Femoral Artery

NCT00933270

COMPLETED

A Prospective Clinical Outcomes Registry

NCT01305525

COMPLETED

SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac Resynchronization Therapy Defibrillator Patients

NCT00940888

COMPLETED Phase 3

SPIRIT PRIME Clinical Trial

NCT00916370

TERMINATED NA

Therapy Cool Path Ablate VT

NCT00925522

TERMINATED NA

BOOST - Benefit of Frequent Optimization After Cardiac Resynchronization Therapy Device Replacement

NCT00929474

COMPLETED NA

Detect Fluid Early From Intra-thoracic Impedance Monitoring

NCT00916929

TERMINATED NA

CONcomitant eValuation of Epicor Left atRial Therapy for AF

NCT00519194

COMPLETED

OptiSense™ Performance in Detecting Atrial Episodes

NCT00870324

COMPLETED Phase 3

Trial to Evaluate the Safety & Efficacy of the Omnilink Elite™ Peripheral Balloon-Expandable Stent System in Subjects With Atherosclerotic de Novo or Restenotic Lesions in the Native Common Iliac Artery and/or Native External Iliac Artery

NCT01396525

COMPLETED Phase 3

Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Expanding Stent System in Subjects With Atherosclerotic de Novo or Restenotic Lesions in the Native Common Iliac Artery and/or Native External Iliac Artery.

NCT00844532

COMPLETED

Comparison of Fixed Tilt and Tuned Waveforms in Right-sided Implants

NCT00873691

COMPLETED

Comparison of 50% Tilt and Tuned Waveforms in Single-Coil Active Can Configuration

NCT00874445

COMPLETED NA

Real World Expanded Multicenter Study of the MitraClip® System (REALISM)

NCT01931956

COMPLETED

Data Collection Study of Wedge Pressure Data in Patients With CRT-D Devices

NCT00811551

COMPLETED

XIENCE V® EXCEED: Evaluation of XIENCE V® Catheterization Lab Endpoints and Excellence in Delivery

NCT00731237

COMPLETED NA

Safety and Efficacy Study of the QuickFlex Micro Model 1258T Left Heart Pacing Lead

NCT00763698

← Previous Page 4 of 6 Next →

Phase Distribution

PhaseTrial count
Phase 1 4
Phase 2 1
Phase 3 11
Phase 4 6

What the Pipeline for Abbott Medical Devices Shows

According to the ClinicalTrials.gov registry, Abbott Medical Devices is linked to 261 US clinical trials across every stage of research activity. Of those, 23 studies are currently recruiting, about 9% of the sponsor's indexed portfolio, and 186 are already marked complete, representing roughly 71% of the total.

The phase mix for Abbott Medical Devices reports 17 late-stage studies (Phase 3 and Phase 4 combined) and 5 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Abbott Medical Devices is Heart Failure with 15 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.