Abbott Medical Devices
Open enrollment with a later-stage pipeline tilt
According to ClinicalTrials.gov-derived indexes, Abbott Medical Devices sits in the top decile of US sponsors by registered trial count (#127 of 15,742 sponsors by registered trial count).
Abbott Medical Devices: 261 sponsored US clinical trials, 23 recruiting.
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.
Top-decile sponsor footprint
Abbott Medical Devices ranks in the top decile of sponsors by registered trial count (#127 of 15,742 sponsors by registered trial count). Volume at this scale usually reflects a long institutional pipeline, read phase tilt and therapeutic areas below before treating it as current-year activity.
Trial completion reliability score
186 of 211 decided trials (Completed vs. Terminated on ClinicalTrials.gov) reached their planned completion (88.2%), vs. national p10 68.4% / p90 100% among 1,234 sponsors with at least 10 decided trials. Still-open trials (Recruiting, Active-not-recruiting, Not-yet-recruiting) are excluded since they have not reached an outcome yet.
Open and recent trials
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
Where Abbott Medical Devices enrollment is open (later-stage tilt)
23 recruiting of 261 indexed (9% open); 186 completed (71%).
Phase mix: 17 late (III/IV) vs 5 early (I/II) (later-stage heavy).
Top condition: Heart Failure (15 trials), 9 others listed.
How open-pipeline share is computed
Recruiting share is recruiting_count divided by trial_count for this sponsor in the public registry export. Status can change between pulls; treat the figure as a research-attention snapshot, not product availability.
Abbott Medical Devices: open-pipeline peers nationwide
Peers matched on 261 registered trials and 9% open enrollment, not the therapeutic-area sidebar.
Abbott Medical Devices sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together.
Sponsors near 261 trials (± recruiting share)
- Pennington Biomedical Research Center · 258 trials · 13% recruiting
- Novartis · 265 trials · 0% recruiting
- University of Texas at Austin · 257 trials · 23% recruiting
- Boston Medical Center · 253 trials · 11% recruiting
Sponsors near 9% open enrollment (± trial volume)
- Grifols Therapeutics · 9% recruiting · 34 trials
- Butler Hospital · 9% recruiting · 103 trials
- AMAG Pharmaceuticals · 9% recruiting · 23 trials
- Iowa State University · 9% recruiting · 23 trials
Related
What to do with this Abbott Medical Devices page
261 registered trials is a research-attention snapshot, not an endorsement of Abbott Medical Devices or any single study.
- 23 of Abbott Medical Devices's trials are currently recruiting, check each one's own eligibility criteria before contacting a site. Browse recruiting trials
- Heart Failure is the condition Abbott Medical Devices studies most, compare against other sponsors active in the same condition before evaluating a specific study. See Heart Failure trials
- Bring the specific trial ID (NCT number) to your own doctor before enrolling, this page is a directory, not medical guidance. Read the trial-finding guide
Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. Abbott Medical Devices pipeline card: 261 registered trials from official public datasets. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.