Abbott Medical Devices
Trial Pipeline
Agilis RF TSP Early Feasibility Study
NCT07361445
Abbott Cephea Mitral Valve Disease Registry
NCT07069673
TriClip CED RWE Study
NCT06920745
TECTONIC CAD IVL IDE Study
NCT06885177
CardioMEMS HF System Coverage with Evidence Development Study
NCT06779552
ViewFlex X ICE First-in-Human Study
NCT06772493
Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in Patients With Advancing Heart Failure
NCT06526195
Esprit BTK Post-Approval Study
NCT06656364
Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND)
NCT06423430
Abbott Structural Heart Device Registry
NCT06590467
Aveir AR Coverage With Evidence Development (CED) Study
NCT06100770
AVEIR DR Coverage With Evidence Development (CED) Study
NCT05932602
Aveir DR Real-World Evidence Post-Approval Study
NCT05935007
External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO)
NCT05537662
Aveir VR Real-World Evidence Post-Approval Study
NCT05270499
Aveir VR Coverage With Evidence Development Post-Approval Study
NCT05336877
Cephea Early Feasibility Study
NCT05061004
Valved Graft PMCF Study
NCT04754217
Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study
NCT04761120
Abbott Vascular Medical Device Registry
NCT04573660
Abbott DBS Post-Market Study of Outcomes for Indications Over Time
NCT04071847
Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator
NCT03876054
Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System for the Treatment of Severe, Symptomatic Aortic Stenosis
NCT07116551
ASCEND CSP IDE Study
NCT06830746
A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PAF:
NCT06676072
Abbott Medical - VERITAS Study
NCT06707688
Assert-IQ Implantable Cardiac Monitor (ICM) Post Market Study
NCT06172699
Abbott Ventricular Tachycardia PAS
NCT05839873
Amulet™ ADVANCE LAA
NCT05997446
Abbott Atrial Fibrillation Post Approval Study
NCT05434650
XIENCE Skypoint Large Vessel Post Approval Study
NCT05423379
Remote Optimization, Adjustment and Measurement for Deep Brain Stimulation
NCT05269862
LIFE-BTK PK Sub-study
NCT05208905
Aveir DR i2i Study
NCT05252702
PARADIGM: Amplatzer Valvular Plug for PVL Closure
NCT04489823
The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System
NCT04559945
LIFE-BTK Randomized Controlled Trial
NCT04227899
MitraClip REPAIR MR Study
NCT04198870
Amplatzer Amulet LAAO vs. NOAC
NCT04226547
JETi Lower Extremity Venous Thrombosis
NCT07027878
MitraClip EXPAND G4 Study
NCT04177394
SJM Masters HP 15mm Rotatable Mechanical Heart Valve as Aortic Valve Replacement Therapy
NCT03924661
SyncAV Post-Market Trial
NCT04100148
Portico Next Generation Approval Study
NCT04011722
TRILUMINATE Pivotal Trial
NCT03904147
Clinical Trial to Evaluate the Safety and Effectiveness of Using the Tendyne Transcatheter Mitral Valve System for the Treatment of Symptomatic Mitral Regurgitation
NCT03433274
Confirm Rx Insertable Cardiac Monitor SMART Registry
NCT03505801
AMPLATZER PFO Occluder Post Approval Study
NCT03309332
Portico Re-sheathable Transcatheter Aortic Valve System US IDE Trial
NCT02000115
Patient Preferences for Leadless Pacemakers
NCT05327101
TactiFlex Paroxysmal Atrial Fibrillation IDE Trial
NCT04356040
Abbott Next Generation Drug Eluting Stent 48mm Study
NCT04282148
LSI (Lesion Index) Workflow Observational Study
NCT03906461
Feasibility Study of the Tendyne Mitral Valve System in Mitral Annular Calcification
NCT03539458
FLExAbility Sensor Enabled Substrate Targeted Ablation for the Reduction of VT Study
NCT03490201
The MitraClip® EXPAND Study of the Next Generation of MitraClip® Devices
NCT03502811
Hemodynamic-GUIDEd Management of Heart Failure
NCT03387813
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
TRILUMINATE Study With Abbott Transcatheter Clip Repair System in Patients With Moderate or Greater TR
NCT03227757
AMPLATZER Duct Occluder II Additional Sizes
NCT03055858
MOMENTUM 3 Continued Access Protocol
NCT02892955
SJM MRI Diagnostic Imaging Registry (IDE)
NCT02807948
A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse VR ICD Undergoing MRI, an IDE Study
NCT02787291
Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE) Study
NCT02548455
OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiography to Guide Coronary Stent Implantation
NCT02471586
TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post Approval Study
NCT02310100
CardioMEMS HF System Post Approval Study
NCT02279888
Randomized Evaluation of Atrial Fibrillation Treatment With Focal Impulse and Rotor Modulation Guided Procedures
NCT02274857
Coronary Orbital Atherectomy System Study
NCT02132611
Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery Lesions
NCT02229864
Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Implant
NCT01993862
CRT Implant Strategy Using the Longest Electrical Delay for Non-left Bundle Branch Block Patients
NCT01983293
Observational Study of OCT in a Patients Undergoing FFR
NCT01663896
Quadripolar Pacing Post Approval Study
NCT01555619
Traumatic Brain Injury Peripheral Nerve Study
NCT01588691
Risk Assessment and Comparative Effectiveness of Left Ventricular Assist Device (LVAD) and Medical Management
NCT01452802
Absolute Pro® MOMENTUM™
NCT01444378
A Clinical Evaluation of the MINI TREK RX 1.20 mm Coronary Dilatation Catheter in Stenotic Lesions
NCT01186198
Left Atrial Pressure Monitoring to Optimize Heart Failure Therapy
NCT01121107
A Prospective Clinical Outcomes Registry
NCT01305525
SJ4 Post Approval Study in Implantable Cardioverter-Defibrillator and Cardiac Resynchronization Therapy Defibrillator Patients
NCT00940888
Detect Fluid Early From Intra-thoracic Impedance Monitoring
NCT00916929
OptiSense™ Performance in Detecting Atrial Episodes
NCT00870324
Programming Implantable Cardioverter Defibrillators in Patients With Primary Prevention Indication
NCT00743522
Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds
NCT00746356
XIENCE V® Everolimus Eluting Coronary Stent System USA Post-Approval Study (XIENCE V® USA Long Term Follow-up Cohort)
NCT01120379
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
'Effect of CRT on Defibrillation Threshold Estimates' Study
NCT00626093
Closure of Atrial Septal Defects With the AMPLATZER Septal Occluder - Post Approval Study
NCT00650936
Cardiac Resynchronization Therapy Defibrillator Based Impedance Monitoring Study
NCT00500838
Aortic Valve Replacement With Trifecta(TM)
NCT00475709
EnSite NavX-Guided Coronary Sinus Mapping During CRT Implant
NCT01615835
SPIRIT IV Clinical Trial: Clinical Evaluation of the XIENCE V® Everolimus Eluting Coronary Stent System
NCT00307047
RISE: A Clinical Evaluation of the StarClose™ Vascular Closure System
NCT00736086
CAPTURE 2 Post-Marketing Registry
NCT00302237
RISK Stratification Using a Combination of Cardiac Troponin T and Brain Natriuretic Peptide in Patients Receiving CRT-D
NCT00453622
Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination Therapy
NCT00121485
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 1 |
| Phase 3 | 1 |
| Phase 4 | 1 |
Therapeutic Areas
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.
Read our methodology — how this data is sourced, computed, and verified.