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 3 of 6
Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients Without Antiplatelet Therapy
NCT02836652
A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgitation Subjects Receiving the MitraClip® Device
NCT02858245
A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditional SCS Systems
NCT02738840
PRESSUREwire Study
NCT02935088
AMPLATZER™ Amulet™ LAA Occluder Trial
NCT02879448
TARGET Post-Approval Study
NCT02800863
MOMENTUM 3 Continued Access Protocol
NCT02892955
MultiPoint Pacing™ Post Market Study
NCT02832622
SJM MRI Diagnostic Imaging Registry (IDE)
NCT02807948
Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With FIRM Guided Procedures
NCT02799043
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
MediGuide Registry
NCT02470312
SHIELD II Clinical Investigation
NCT02468778
HALO: A Single Arm Prospective Investigation of the SJM™ Masters HP™ 15mm Rotatable Mechanical Heart Valve
NCT02097420
OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiography to Guide Coronary Stent Implantation
NCT02471586
Coronary Flow Reserve Following Orbital Atherectomy
NCT02339545
TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post Approval Study
NCT02310100
ADVANCE ASO AMPLATZER™ Atrial Septal Occluder Post Market Surveillance Study
NCT02353351
CardioMEMS HF System Post Approval Study
NCT02279888
Expanded Clinical Study of the Tendyne Mitral Valve System
NCT02321514
Substrate Targeted Ablation Using the FlexAbility™ Ablation Catheter System for the Reduction of Ventricular Tachycardia
NCT02130765
Randomized Evaluation of Atrial Fibrillation Treatment With Focal Impulse and Rotor Modulation Guided Procedures
NCT02274857
MOMENTUM 3 IDE Clinical Study Protocol
NCT02224755
PREVENtion of HeartMate II Pump Thrombosis
NCT02158403
Optisure Lead Post Approval Study
NCT02235545
Absorb IV Randomized Controlled Trial
NCT02173379
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
The LEADLESS II IDE Study for the Nanostim Leadless Pacemaker
NCT02030418
SUNBURST (Success Using Neuromodulation With BURST) Study
NCT02011893
MOre REsponse on Cardiac Resynchronization Therapy With MultiPoint Pacing
NCT02006069
CRT Implant Strategy Using the Longest Electrical Delay for Non-left Bundle Branch Block Patients
NCT01983293
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
NCT01990287
EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hypertension
NCT01903187
Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely Calcified Coronary Lesions (MACE)
NCT01930214
Remote Device Interrogation In The Emergency Department
NCT01871090
A Safety and Effectiveness Trial of Spinal Cord Stimulation of the Dorsal Root Ganglion for Chronic Lower Limb Pain
NCT01923285
A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) System in Chinese Population ~ ABSORB CHINA Randomized Controlled Trial (RCT)
NCT01923740
XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm Study
NCT01894152
Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes
NCT01855412
MultiPoint Pacing IDE Study
NCT01786993
Complete Lesion Assessment With ffR and IVUS TechnologY
NCT01941030
St.Jude Medical Cardiac Lead Assessment Study
NCT01507987
Advance Cardiac Resynchronization Therapy (CRT) Registry
NCT01805154
Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal
NCT01938391
Safety Study on Stopping Anticoagulation Medication in Patients With a History of Atrial Fibrillation
NCT01650298
Observational Study of OCT in a Patients Undergoing FFR
NCT01663896
ABSORB III Randomized Controlled Trial (RCT)
NCT01751906
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.