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 3 of 6

COMPLETED Phase 4

Prevention of Non-Surgical Bleeding by Management of HeartMate II Patients Without Antiplatelet Therapy

NCT02836652

TERMINATED

A Feasibility Registry of Actigraphy Monitoring in Degenerative Mitral Regurgitation Subjects Receiving the MitraClip® Device

NCT02858245

COMPLETED NA

A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditional SCS Systems

NCT02738840

COMPLETED

PRESSUREwire Study

NCT02935088

COMPLETED NA

AMPLATZER™ Amulet™ LAA Occluder Trial

NCT02879448

COMPLETED

TARGET Post-Approval Study

NCT02800863

COMPLETED NA

MOMENTUM 3 Continued Access Protocol

NCT02892955

COMPLETED

MultiPoint Pacing™ Post Market Study

NCT02832622

COMPLETED NA

SJM MRI Diagnostic Imaging Registry (IDE)

NCT02807948

COMPLETED NA

Randomized Evaluation of Redo Ablation Procedures of Atrial Fibrillation With FIRM Guided Procedures

NCT02799043

COMPLETED NA

A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse VR ICD Undergoing MRI, an IDE Study

NCT02787291

COMPLETED NA

Quartet 1457Q Left Ventricular (LV) Lead Investigational Device Exemption (IDE) Study

NCT02548455

TERMINATED

MediGuide Registry

NCT02470312

TERMINATED NA

SHIELD II Clinical Investigation

NCT02468778

COMPLETED NA

HALO: A Single Arm Prospective Investigation of the SJM™ Masters HP™ 15mm Rotatable Mechanical Heart Valve

NCT02097420

COMPLETED NA

OPTIMIZE PCI: Multicenter Randomized Trial of OCT Compared to IVUS and Angiography to Guide Coronary Stent Implantation

NCT02471586

COMPLETED

Coronary Flow Reserve Following Orbital Atherectomy

NCT02339545

COMPLETED NA

TactiCath® Contact Force Ablation Catheter Study for Atrial Fibrillation Post Approval Study

NCT02310100

TERMINATED

ADVANCE ASO AMPLATZER™ Atrial Septal Occluder Post Market Surveillance Study

NCT02353351

COMPLETED

CardioMEMS HF System Post Approval Study

NCT02279888

COMPLETED NA

Expanded Clinical Study of the Tendyne Mitral Valve System

NCT02321514

TERMINATED NA

Substrate Targeted Ablation Using the FlexAbility™ Ablation Catheter System for the Reduction of Ventricular Tachycardia

NCT02130765

COMPLETED NA

Randomized Evaluation of Atrial Fibrillation Treatment With Focal Impulse and Rotor Modulation Guided Procedures

NCT02274857

COMPLETED NA

MOMENTUM 3 IDE Clinical Study Protocol

NCT02224755

COMPLETED NA

PREVENtion of HeartMate II Pump Thrombosis

NCT02158403

TERMINATED

Optisure Lead Post Approval Study

NCT02235545

COMPLETED NA

Absorb IV Randomized Controlled Trial

NCT02173379

COMPLETED NA

Coronary Orbital Atherectomy System Study

NCT02132611

COMPLETED NA

Pharmacokinetics of Everolimus in Absorb BVS in Patients With Coronary Artery Lesions

NCT02229864

COMPLETED NA

Same Day Discharge (SDD) After Implantable Cardioverter Defibrillator (ICD) Implant

NCT01993862

COMPLETED NA

The LEADLESS II IDE Study for the Nanostim Leadless Pacemaker

NCT02030418

COMPLETED NA

SUNBURST (Success Using Neuromodulation With BURST) Study

NCT02011893

TERMINATED NA

MOre REsponse on Cardiac Resynchronization Therapy With MultiPoint Pacing

NCT02006069

COMPLETED NA

CRT Implant Strategy Using the Longest Electrical Delay for Non-left Bundle Branch Block Patients

NCT01983293

TERMINATED NA

SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study

NCT01990287

TERMINATED NA

EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hypertension

NCT01903187

COMPLETED

Multi-center Prospective Study to Evaluate Outcomes of the Moderate to Severely Calcified Coronary Lesions (MACE)

NCT01930214

COMPLETED NA

Remote Device Interrogation In The Emergency Department

NCT01871090

COMPLETED NA

A Safety and Effectiveness Trial of Spinal Cord Stimulation of the Dorsal Root Ganglion for Chronic Lower Limb Pain

NCT01923285

COMPLETED NA

A Clinical Evaluation of Absorb™ Bioresorbable Vascular Scaffold (Absorb™ BVS) System in Chinese Population ~ ABSORB CHINA Randomized Controlled Trial (RCT)

NCT01923740

COMPLETED

XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm Study

NCT01894152

COMPLETED

Observational Study to Evaluate PAD Treatment Clinical and Economic Outcomes

NCT01855412

COMPLETED Phase 3

MultiPoint Pacing IDE Study

NCT01786993

COMPLETED NA

Complete Lesion Assessment With ffR and IVUS TechnologY

NCT01941030

COMPLETED

St.Jude Medical Cardiac Lead Assessment Study

NCT01507987

COMPLETED

Advance Cardiac Resynchronization Therapy (CRT) Registry

NCT01805154

COMPLETED NA

Tissue Removal Assessment With Ultrasound of THe SFA and Popliteal

NCT01938391

TERMINATED NA

Safety Study on Stopping Anticoagulation Medication in Patients With a History of Atrial Fibrillation

NCT01650298

COMPLETED

Observational Study of OCT in a Patients Undergoing FFR

NCT01663896

COMPLETED NA

ABSORB III Randomized Controlled Trial (RCT)

NCT01751906

← Previous Page 3 of 6 Next →

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.