Abbott Medical Devices

155 total trials 76 currently recruiting 52 completed

Trial Pipeline

RECRUITING NA

Agilis RF TSP Early Feasibility Study

NCT07361445

RECRUITING

Abbott Cephea Mitral Valve Disease Registry

NCT07069673

RECRUITING

TriClip CED RWE Study

NCT06920745

RECRUITING NA

TECTONIC CAD IVL IDE Study

NCT06885177

RECRUITING

CardioMEMS HF System Coverage with Evidence Development Study

NCT06779552

RECRUITING

ViewFlex X ICE First-in-Human Study

NCT06772493

RECRUITING NA

Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in Patients With Advancing Heart Failure

NCT06526195

RECRUITING NA

Esprit BTK Post-Approval Study

NCT06656364

RECRUITING NA

Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND)

NCT06423430

RECRUITING

Abbott Structural Heart Device Registry

NCT06590467

RECRUITING

Aveir AR Coverage With Evidence Development (CED) Study

NCT06100770

RECRUITING

AVEIR DR Coverage With Evidence Development (CED) Study

NCT05932602

RECRUITING

Aveir DR Real-World Evidence Post-Approval Study

NCT05935007

RECRUITING NA

External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO)

NCT05537662

RECRUITING

Aveir VR Real-World Evidence Post-Approval Study

NCT05270499

RECRUITING

Aveir VR Coverage With Evidence Development Post-Approval Study

NCT05336877

RECRUITING NA

Cephea Early Feasibility Study

NCT05061004

RECRUITING

Valved Graft PMCF Study

NCT04754217

RECRUITING

Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study

NCT04761120

RECRUITING

Abbott Vascular Medical Device Registry

NCT04573660

RECRUITING

Abbott DBS Post-Market Study of Outcomes for Indications Over Time

NCT04071847

RECRUITING

Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator

NCT03876054

ACTIVE NOT RECRUITING NA

Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System for the Treatment of Severe, Symptomatic Aortic Stenosis

NCT07116551

ACTIVE NOT RECRUITING NA

ASCEND CSP IDE Study

NCT06830746

ACTIVE NOT RECRUITING NA

A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PAF:

NCT06676072

ACTIVE NOT RECRUITING NA

Abbott Medical - VERITAS Study

NCT06707688

ACTIVE NOT RECRUITING

Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study

NCT06172699

ACTIVE NOT RECRUITING

Abbott Ventricular Tachycardia PAS

NCT05839873

ACTIVE NOT RECRUITING

Amulet™ ADVANCE LAA

NCT05997446

ACTIVE NOT RECRUITING

Abbott Atrial Fibrillation Post Approval Study

NCT05434650

ACTIVE NOT RECRUITING

XIENCE Skypoint Large Vessel Post Approval Study

NCT05423379

ACTIVE NOT RECRUITING NA

Remote Optimization, Adjustment and Measurement for Deep Brain Stimulation

NCT05269862

ACTIVE NOT RECRUITING NA

LIFE-BTK PK Sub-study

NCT05208905

ACTIVE NOT RECRUITING NA

Aveir DR i2i Study

NCT05252702

ACTIVE NOT RECRUITING NA

PARADIGM: Amplatzer Valvular Plug for PVL Closure

NCT04489823

ACTIVE NOT RECRUITING NA

The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System

NCT04559945

ACTIVE NOT RECRUITING NA

LIFE-BTK Randomized Controlled Trial

NCT04227899

ACTIVE NOT RECRUITING NA

MitraClip REPAIR MR Study

NCT04198870

ACTIVE NOT RECRUITING NA

Amplatzer Amulet LAAO vs. NOAC

NCT04226547

ACTIVE NOT RECRUITING

JETi Lower Extremity Venous Thrombosis

NCT07027878

ACTIVE NOT RECRUITING

MitraClip EXPAND G4 Study

NCT04177394

ACTIVE NOT RECRUITING

SJM Masters HP 15mm Rotatable Mechanical Heart Valve as Aortic Valve Replacement Therapy

NCT03924661

ACTIVE NOT RECRUITING NA

SyncAV Post-Market Trial

NCT04100148

ACTIVE NOT RECRUITING NA

Portico Next Generation Approval Study

NCT04011722

ACTIVE NOT RECRUITING NA

TRILUMINATE Pivotal Trial

NCT03904147

ACTIVE NOT RECRUITING NA

Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Transcatheter Mitral Valve System for the Treatment of Symptomatic Mitral Regurgitation

NCT03433274

ACTIVE NOT RECRUITING

Confirm Rx Insertable Cardiac Monitor SMART Registry

NCT03505801

ACTIVE NOT RECRUITING NA

AMPLATZER PFO Occluder Post Approval Study

NCT03309332

ACTIVE NOT RECRUITING NA

Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial

NCT02000115

COMPLETED

Patient Preferences for Leadless Pacemakers

NCT05327101

COMPLETED NA

TactiFlex Paroxysmal Atrial Fibrillation IDE Trial

NCT04356040

COMPLETED NA

Abbott Next Generation Drug Eluting Stent 48mm Study

NCT04282148

COMPLETED

LSI (Lesion Index) Workflow Observational Study

NCT03906461

COMPLETED NA

Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcification

NCT03539458

COMPLETED NA

FLExAbility Sensor Enabled Substrate Targeted Ablation for the Reduction of VT Study

NCT03490201

COMPLETED

The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices

NCT03502811

COMPLETED NA

Hemodynamic-GUIDEd Management of Heart Failure

NCT03387813

COMPLETED NA

Cardiovascular Outcomes Assessment of the MitraClip Percutaneous Therapy for Heart Failure Patients With Functional MR

NCT07227675

COMPLETED NA

Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therapy During the Trial

NCT03277378

COMPLETED

EnSite Precision Observational Study

NCT03260244

COMPLETED NA

TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With Moderate or Greater TR

NCT03227757

COMPLETED NA

AMPLATZER Duct Occluder II Additional Sizes

NCT03055858

COMPLETED NA

MOMENTUM 3 Continued Access Protocol

NCT02892955

COMPLETED NA

SJM MRI Diagnostic Imaging Registry (IDE)

NCT02807948

COMPLETED NA

A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse VR ICD Undergoing MRI, an IDE Study

NCT02787291

COMPLETED NA

Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE) Study

NCT02548455

COMPLETED NA

OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiography to Guide Coronary Stent Implantation

NCT02471586

COMPLETED NA

TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post Approval Study

NCT02310100

COMPLETED

CardioMEMS HF System Post Approval Study

NCT02279888

COMPLETED NA

Randomized Evaluation of Atrial Fibrillation Treatment With Focal Impulse and Rotor Modulation Guided Procedures

NCT02274857

COMPLETED NA

Coronary Orbital Atherectomy System Study

NCT02132611

COMPLETED NA

Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery Lesions

NCT02229864

COMPLETED NA

Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Implant

NCT01993862

COMPLETED NA

CRT Implant Strategy Using the Longest Electrical Delay for Non-left Bundle Branch Block Patients

NCT01983293

COMPLETED

Observational Study of OCT in a Patients Undergoing FFR

NCT01663896

COMPLETED

Quadripolar Pacing Post Approval Study

NCT01555619

COMPLETED Phase 1

Traumatic Brain Injury Peripheral Nerve Study

NCT01588691

COMPLETED

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

NCT01452802

COMPLETED NA

Absolute Pro® MOMENTUM™

NCT01444378

COMPLETED

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

NCT01186198

COMPLETED NA

Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy

NCT01121107

COMPLETED

A Prospective Clinical Outcomes Registry

NCT01305525

COMPLETED

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

NCT00940888

COMPLETED NA

Detect Fluid Early From Intra-thoracic Impedance Monitoring

NCT00916929

COMPLETED

OptiSense™ Performance in Detecting Atrial Episodes

NCT00870324

COMPLETED

Programming Implantable Cardioverter Defibrillators in Patients With Primary Prevention Indication

NCT00743522

COMPLETED NA

Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds

NCT00746356

COMPLETED

XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIENCE V® USA Long Term Follow-up Cohort)

NCT01120379

COMPLETED

Patient Centered Machine Learning Model for Bleeding and Ischemic Risk

NCT06089304

COMPLETED NA

Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscular VSD (MuVSD) Occluder - Post Approval Study

NCT00647387

COMPLETED Phase 4

'Effect of CRT on Defibrillation Threshold Estimates' Study

NCT00626093

COMPLETED NA

Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Approval Study

NCT00650936

COMPLETED NA

Cardiac Resynchronization Therapy Defibrillator Based Impedance Monitoring Study

NCT00500838

COMPLETED NA

Aortic Valve Replacement With Trifecta(TM)

NCT00475709

COMPLETED NA

EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant

NCT01615835

COMPLETED Phase 3

SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary Stent System

NCT00307047

COMPLETED

RISE: A Clinical Evaluation of the StarClose™ Vascular Closure System

NCT00736086

COMPLETED

CAPTURE 2 Post-Marketing Registry

NCT00302237

COMPLETED

RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriuretic Peptide in Patients Receiving CRT-D

NCT00453622

COMPLETED NA

Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination Therapy

NCT00121485

What the Pipeline for Abbott Medical Devices Shows

According to the ClinicalTrials.gov registry, Abbott Medical Devices is linked to 155 US clinical trials across every stage of research activity. Of those, 76 studies are currently recruiting — about 49% of the sponsor's indexed portfolio — and 52 are already marked complete, representing roughly 34% of the total. 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.

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

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. 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.

Related

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