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 2 of 6

COMPLETED

AVEIR Remote Care System Non-Significant Risk Study

NCT06542133

COMPLETED NA

VOLT-AF IDE Clinical Study

NCT06223789

COMPLETED

LBBAP Data Collection Registry

NCT05887323

COMPLETED

Validation of CardioMEMS HF System Cardiac Output Algorithm IDE

NCT05428384

COMPLETED

Patient Preferences for Leadless Pacemakers

NCT05327101

COMPLETED

ECGi of SyncAV With MultiPoint Pacing

NCT06444386

COMPLETED NA

Perclose Multi-Access Duplex Ultrasound (DUS) Study

NCT04904809

COMPLETED

Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation

NCT04873817

COMPLETED

Spinal Cord Stimulation Trial to Permanent Prediction

NCT05659836

COMPLETED

CentriMag Failure-to-Wean Post Approval Study

NCT04464785

COMPLETED

Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical SWIFT HM3 PMS

NCT04548128

COMPLETED NA

Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT)

NCT04479787

COMPLETED NA

The ARIES HeartMate 3 Pump IDE Study

NCT04069156

COMPLETED NA

TactiFlex Paroxysmal Atrial Fibrillation IDE Trial

NCT04356040

COMPLETED

FUnctional diagnoSIs of corONary Stenosis (FUSION)

NCT04356027

COMPLETED NA

Abbott Next Generation Drug Eluting Stent 48mm Study

NCT04282148

COMPLETED

JETi Lower Extremity Arterial Thrombosis

NCT04370691

COMPLETED NA

Evaluation of the Infinity Deep Brain Stimulation Electrode Screening Mode Tool

NCT03794661

COMPLETED

MOMENTUM 3 Pivotal Cohort Extended Follow-up PAS

NCT03982979

COMPLETED

Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Intervention: REACH PVI

NCT03943160

COMPLETED

LSI (Lesion Index) Workflow Observational Study

NCT03906461

COMPLETED NA

PROLONG Prospective, Multi-center, Open-label, Post-market Study

NCT03908476

COMPLETED

A Post-Market Study Evaluating the Safety of Infinity DBS System With MR Conditional Labeling

NCT03884231

COMPLETED NA

Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundle Branch Block

NCT03803995

COMPLETED NA

XIENCE 28 USA Study

NCT03815175

COMPLETED

Physiologic Pacing Registry

NCT03719040

COMPLETED NA

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

NCT03539458

COMPLETED

The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption (H070005) Post Approval Study

NCT03165526

COMPLETED NA

Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCath SE) Catheter for Ablation of Drug Refractory, Symptomatic, Persistent Atrial Fibrillation

NCT03650556

COMPLETED

HBP Device EGM Data Collection

NCT03564860

COMPLETED

Intraoperative Investigation of a Directional Lead and Local Field Potentials for the Optimization of Stimulation Efficacy

NCT03630302

COMPLETED NA

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

NCT03490201

COMPLETED NA

ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI)

NCT03507777

COMPLETED

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

NCT03502811

COMPLETED NA

Hemodynamic-GUIDEd Management of Heart Failure

NCT03387813

COMPLETED NA

TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation

NCT03354663

COMPLETED NA

BurstDR™ micrOdosing stimuLation in De-novo Patients

NCT03350256

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

Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Devices Using the CardioMEMS™

NCT03247829

COMPLETED NA

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

NCT03227757

COMPLETED NA

XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HBR Patients.

NCT03218787

TERMINATED

SJM Brady MRI Post Approval Study

NCT03170583

COMPLETED NA

AMPLATZER Duct Occluder II Additional Sizes

NCT03055858

COMPLETED

IPG Replacement Study (PREFERENCE-H)

NCT02963259

COMPLETED NA

Trifecta™ GT Post Market Clinical Follow-up

NCT03016169

COMPLETED NA

Multi-center Prospective Study Determining the Sustainability of Pain Relief and Psychosocial and Functional Responses When Utilizing a Multiple Waveform Enabled Neurostimulator

NCT03082261

COMPLETED

Clinical Evaluation of the Infinity Deep Brain Stimulation System

NCT02989610

COMPLETED

The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchronization Therapy

NCT02903940

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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.