Abbott Medical Devices
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
AVEIR Remote Care System Non-Significant Risk Study
NCT06542133
VOLT-AF IDE Clinical Study
NCT06223789
LBBAP Data Collection Registry
NCT05887323
Validation of CardioMEMS HF System Cardiac Output Algorithm IDE
NCT05428384
Patient Preferences for Leadless Pacemakers
NCT05327101
ECGi of SyncAV With MultiPoint Pacing
NCT06444386
Perclose Multi-Access Duplex Ultrasound (DUS) Study
NCT04904809
Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation
NCT04873817
Spinal Cord Stimulation Trial to Permanent Prediction
NCT05659836
CentriMag Failure-to-Wean Post Approval Study
NCT04464785
Implantation of the HeartMate 3 in Subjects With Heart Failure Using Surgical SWIFT HM3 PMS
NCT04548128
Spinal Cord Stimulation vs. Medical Management for Low Back Pain (DISTINCT)
NCT04479787
The ARIES HeartMate 3 Pump IDE Study
NCT04069156
TactiFlex Paroxysmal Atrial Fibrillation IDE Trial
NCT04356040
FUnctional diagnoSIs of corONary Stenosis (FUSION)
NCT04356027
Abbott Next Generation Drug Eluting Stent 48mm Study
NCT04282148
JETi Lower Extremity Arterial Thrombosis
NCT04370691
Evaluation of the Infinity Deep Brain Stimulation Electrode Screening Mode Tool
NCT03794661
MOMENTUM 3 Pivotal Cohort Extended Follow-up PAS
NCT03982979
Radial accEss for nAvigation to Your CHosen Lesion for Peripheral Vascular Intervention: REACH PVI
NCT03943160
LSI (Lesion Index) Workflow Observational Study
NCT03906461
PROLONG Prospective, Multi-center, Open-label, Post-market Study
NCT03908476
A Post-Market Study Evaluating the Safety of Infinity DBS System With MR Conditional Labeling
NCT03884231
Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundle Branch Block
NCT03803995
XIENCE 28 USA Study
NCT03815175
Physiologic Pacing Registry
NCT03719040
Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcification
NCT03539458
The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption (H070005) Post Approval Study
NCT03165526
Safety and Effectiveness of TactiCath™ Contact Force, Sensor Enabled™ (TactiCath SE) Catheter for Ablation of Drug Refractory, Symptomatic, Persistent Atrial Fibrillation
NCT03650556
HBP Device EGM Data Collection
NCT03564860
Intraoperative Investigation of a Directional Lead and Local Field Potentials for the Optimization of Stimulation Efficacy
NCT03630302
FLExAbility Sensor Enabled Substrate Targeted Ablation for the Reduction of VT Study
NCT03490201
ILUMIEN IV: OPTIMAL Percutaneous Coronary Intervention (PCI)
NCT03507777
The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices
NCT03502811
Hemodynamic-GUIDEd Management of Heart Failure
NCT03387813
TactiSense IDE Trial of TactiCath SE for Paroxysmal Atrial Fibrillation
NCT03354663
BurstDR™ micrOdosing stimuLation in De-novo Patients
NCT03350256
Cardiovascular Outcomes Assessment of the MitraClip Percutaneous Therapy for Heart Failure Patients With Functional MR
NCT07227675
Evaluating Anatomic Versus Targeted Lead Placement for Burst Stimulation Therapy During the Trial
NCT03277378
EnSite Precision Observational Study
NCT03260244
Investigation to Optimize Hemodynamic Management of Left Ventricular Assist Devices Using the CardioMEMS™
NCT03247829
TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With Moderate or Greater TR
NCT03227757
XIENCE 90: A Safety Evaluation of 3-month DAPT After XIENCE Implantation for HBR Patients.
NCT03218787
SJM Brady MRI Post Approval Study
NCT03170583
AMPLATZER Duct Occluder II Additional Sizes
NCT03055858
IPG Replacement Study (PREFERENCE-H)
NCT02963259
Trifecta™ GT Post Market Clinical Follow-up
NCT03016169
Multi-center Prospective Study Determining the Sustainability of Pain Relief and Psychosocial and Functional Responses When Utilizing a Multiple Waveform Enabled Neurostimulator
NCT03082261
Clinical Evaluation of the Infinity Deep Brain Stimulation System
NCT02989610
The Application of Negative Atrioventricular Hysteresis in Cardiac Resynchronization Therapy
NCT02903940
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 4 |
| Phase 2 | 1 |
| Phase 3 | 11 |
| Phase 4 | 6 |
Therapeutic Areas
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.
Read our methodology - how this data is sourced, computed, and verified.
Related
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.