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 5 of 6
CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulmonary Bypass
NCT00819793
SPIRIT Small Vessel Registry
NCT00783796
Programming Implantable Cardioverter Defibrillators in Patients With Primary Prevention Indication
NCT00743522
Study of New Implantable Loop Recorder
NCT00746564
Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds
NCT00746356
AMPLATZER Duct Occluder II Clinical Study
NCT00713700
XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIENCE V® USA Long Term Follow-up Cohort)
NCT01120379
Angio-Seal Evolution Device Registry
NCT00817349
XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIENCE V® USA-Phase 1)
NCT00676520
Patient Centered Machine Learning Model for Bleeding and Ischemic Risk
NCT06089304
Closure of Muscular Ventricular Septal Defects (VSDs) With the AMPLATZER Muscular VSD (MuVSD) Occluder - Post Approval Study
NCT00647387
Deep Brain Stimulation for Major Depressive Disorder
NCT00617162
Gen2 Isthmus-Dependent Atrial Flutter Ablation Study
NCT00606463
'Effect of CRT on Defibrillation Threshold Estimates' Study
NCT00626093
Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study
NCT00632372
EnSite Real-Time Cardiac Performance Measurements (RT CPM) Study
NCT00632450
St. Jude Medical Product Longevity and Performance (SCORE) Registry
NCT01754064
Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Approval Study
NCT00650936
The HERCULES Trial - A Safety and Effectiveness Study of the Herculink Elite Renal Stent to Treat Renal Artery Stenosis
NCT00490841
Cardiac Resynchronization Therapy Defibrillator Based Impedance Monitoring Study
NCT00500838
Dynamic Substrate Mapping (DSM) for Ischemic VT
NCT00558857
Aortic Valve Replacement With Trifecta(TM)
NCT00475709
AVJ Ablation Followed by Resynchronization Therapy in Patients With CHF and AF
NCT00547794
DEfibrillators To REduce Risk by MagnetIc ResoNance Imaging Evaluation
NCT00487279
EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant
NCT01615835
Aortic or Mitral Valve Replacement With the Biocor and Biocor Supra
NCT00636987
EVEREST II Pivotal Study High Risk Registry (HRR)
NCT01940120
Protected Carotid Artery Stenting in Subjects at High Risk for Carotid Endarterectomy (CEA) (PROTECT)
NCT00402740
RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) Episodes in the Cardiac Rhythm Management (CRM) Device Population
NCT00837798
FREEDOM - A Frequent Optimization Study Using the QuickOpt Method
NCT00418314
CHOICE: Carotid Stenting For High Surgical-Risk Patients
NCT00406055
SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary Stent System
NCT00307047
Lead Registry for Optim Leads
NCT01722188
POWER (Pulse Width Optimized Waveform Evaluation Trial)
NCT00311181
RISE: A Clinical Evaluation of the StarClose™ Vascular Closure System
NCT00736086
CAPTURE 2 Post-Marketing Registry
NCT00302237
Reduction of Right Ventricular Pacing Using the Feature Ventricular Intrinsic Preference (VIP)
NCT00311168
PREMIUM Migraine Trial
NCT00355056
RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriuretic Peptide in Patients Receiving CRT-D
NCT00453622
ESCAPE Migraine Trial
NCT00267371
Deep Brain Stimulation (DBS) for the Suppression of Tremor
NCT02087046
Deep Brain Stimulation to Treat Symptoms of Parkinson's Disease
NCT00552474
Pivotal Study of a Percutaneous Mitral Valve Repair System
NCT00209274
RethinQ Study - Evaluating Pacing in Heart Failure Patients
NCT00132977
Reduce Ventricular Pacing in Dual Chamber Implantable Cardioverter Defibrillators Using AutoIntrinsic Conduction Search Study
NCT00187239
SPIRIT III Clinical Trial of the XIENCE V® Everolimus Eluting Coronary Stent System (EECSS)
NCT00180479
Safety and Efficacy of the ZoMaxx™ Drug-Eluting Stent System in Coronary Arteries
NCT00140101
Carotid Angioplasty and Stenting Versus Endarterectomy in Asymptomatic Subjects Who Are at Standard Risk for Carotid Endarterectomy With Significant Extracranial Carotid Stenotic Disease (ACT I)
NCT00106938
Hemodynamically Guided Home Self-Therapy in Severe Heart Failure Patients (HOMEOSTASIS)
NCT00547729
Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Bridge to Cardiac Transplantation
NCT00121472
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.