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Pharmaceutical sponsor

Abbott Medical Devices Clinical Trials

Studies where Abbott Medical Devices is the lead sponsor: its pipeline by phase, what is enrolling now and where. Studies it supports as a collaborator are in the search.

539 registered studies

In numbers

Open to volunteers
32
Active
68
With results posted
272
All registered
539

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 32
  • Atrial Fibrillation (AF), Paroxysmal AF

    Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration

    • Recruiting
    • Age: 18 years and older
    • Medical device
    • Surgery or procedure

    The objective of this clinical investigation is to evaluate the feasibility, safety, and effectiveness of a concomitant procedure involving the Volt PFA System and Amulet 2 device in patients indicated for both AF ablation and…

    Conditions
    Atrial Fibrillation (AF), Paroxysmal AF, Persistent Atrial Fibrillation
    Trial name
    CLEAR (NCT07523620)
    Testing
    PVI Ablation, Left Atrial Appendage Occluder Implant
    Where
    16 sites in Belgium, Czechia and 8 more
    Volunteers
    240 people
    Sponsor
    Abbott Medical Devices
    Can I take part? CLEAR
  • Cardiac Pacemaker, Arrhythmia

    Aveir AR Coverage With Evidence Development (CED) Study

    • Recruiting
    • Age: 18 years and older
    • Observational study
    • Medical device

    The purpose of this coverage with evidence development (CED) study is to evaluate complications and long-term health outcomes of the single-chamber Aveir Atrial Leadless Pacemaker device (aka Aveir™ AR LP system).

    Conditions
    Cardiac Pacemaker, Arrhythmia, Bradycardia
    Trial name
    ARRIVE (NCT06100770)
    Testing
    Aveir AR Leadless Pacemaker, Single-chamber atrial transvenous pacemaker
    Where
    United States
    Volunteers
    586 people
    Sponsor
    Abbott Medical Devices
    Can I take part? ARRIVE
  • Treatment Resistant Depression

    Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND)

    • Recruiting
    • Age: 22 to 70 years
    • Medical device

    The goal of this clinical trial is to evaluate the effectiveness and safety of bilateral stimulation of the subcallosal cingulate white matter (SCCwm) using Deep Brain Stimulation (DBS) as an adjunctive treatment of non-psychotic…

    Trial name
    TRANSCEND (NCT06423430)
    Testing
    Active-stimulation
    Where
    26 sites in United States
    Volunteers
    100 people
    Sponsor
    Abbott Medical Devices
    Can I take part? TRANSCEND
  • Cardiac Pacemaker, Cardiac Rhythm Disorder

    LEAP 2 Chronic EFS

    • Recruiting
    • Age: 18 years and older
    • Medical device

    Prospective, single-arm, non-randomized, unblinded, chronic feasibility study designed to evaluate the safety and performance of the AVEIR™ Conduction System Pacing (CSP) Leadless Pacemaker system.

    Conditions
    Cardiac Pacemaker, Cardiac Rhythm Disorder, Bradycardia
    Trial name
    NCT07287423
    Testing
    AVEIR CSP Leadless Pacemaker System
    Where
    Czechia
    Volunteers
    30 people
    Sponsor
    Abbott Medical Devices
    Can I take part? NCT07287423
  • Ventricular Tachycardia

    Evaluation of the DuoVT PFA System for Ventricular Tachycardia

    • Recruiting
    • Age: 18 to 80 years
    • Medical device

    This study is a prospective, non-randomized, single-arm, multicenter study to evaluate the safety and effectiveness of the DuoVT Pulsed Field Ablation (PFA) System.

    Trial name
    EXACT-VT (NCT07706712)
    Testing
    Ablation procedure with DuoVT PFA system
    Where
    5 sites in Croatia, Czechia and 2 more
    Volunteers
    50 people
    Sponsor
    Abbott Medical Devices
    Can I take part? EXACT-VT
  • Heart Failure, Bradycardia

    Merlin Expanded ECG NSR

    • Not yet recruiting
    • Age: 18 years and older
    • Observational study
    • Medical device

    This clinical investigation is a prospective, single-arm, multi-center, observational study designed to evaluate the concordance between a simplified electrocardiogram (ECG) method implemented on the Merlin™ 3650 or MER3700…

    Trial name
    NCT07877805
    Testing
    Left Bundle Branch Implant
    Volunteers
    50 people
    Sponsor
    Abbott Medical Devices
    Can I take part? NCT07877805
  • Acute Myocardial Infarction, Restenoses, Coronary

    Abbott Vascular Medical Device Registry

    • Recruiting
    • Age: 18 years and older
    • Observational study
    • Medical device

    The AV-MDR is a prospective, non-randomized, open-label, multi-center registry. The purpose of the AV-MDR study is to proactively collect and evaluate clinical data on the usage of the devices in scope within their intended use…

    Conditions
    Acute Myocardial Infarction, Restenoses, Coronary, Coronary Artery Lesions, Venous Embolism
    Trial name
    AV-MDR (NCT04573660)
    Testing
    Coronary and peripheral stents, Pacing catheters, Vascular plugs
    Where
    37 sites in United States, Australia and 12 more
    Volunteers
    3,784 people
    Sponsor
    Abbott Medical Devices
    Can I take part? AV-MDR
  • Tricuspid Regurgitation (TR)

    A Post-Market Assessment of the Safety and Performance of the TriClip™ System

    • Recruiting
    • Age: 18 years and older
    • Observational study
    • Medical device

    The objective of the TREAT TR study is to confirm the safety and performance of the TriClip System for tricuspid TEER in a contemporary, real-world setting, using the commercially available device in accordance with its approved…

    Trial name
    TREAT TR (NCT07586995)
    Testing
    Tricuspid Transcatheter Edge-to-Edge Repair (TEER)
    Where
    9 sites in United States, Germany and 2 more
    Volunteers
    1,000 people
    Sponsor
    Abbott Medical Devices
    Can I take part? TREAT TR
  • Bradycardia, Right Ventricular Pacing

    Left Bundle Branch Area Pacing (LBBAP) PMCF Study

    • Recruiting
    • Age: 18 years and older
    • Medical device

    The objective of this study is to evaluate the safety and effectiveness of LBBA pacing/sensing in patients implanted with the Tendril STS 2088TC or UltiPace LPA1231 lead through 6 months post-implant.

    Conditions
    Bradycardia, Right Ventricular Pacing, Heart Failure, Atrial Fibrillation (AF)
    Trial name
    LBBAP PMCF (NCT07217392)
    Testing
    LBBAP lead
    Where
    15 sites in Brazil, France and 7 more
    Volunteers
    200 people
    Sponsor
    Abbott Medical Devices
    Can I take part? LBBAP PMCF
  • Mitral Regurgitation

    Cephea Early Feasibility Study

    • Recruiting
    • Age: 18 years and older
    • Medical device

    The objective of this study is to evaluate the preliminary safety and effectiveness of the Cephea Mitral Valve System for the treatment of symptomatic patients with mitral valve disease (including mitral regurgitation, mitral…

    Trial name
    NCT05061004
    Testing
    Cephea Mitral Valve System
    Where
    22 sites in United States, Canada
    Volunteers
    90 people
    Sponsor
    Abbott Medical Devices
    Can I take part? NCT05061004

Completed, with results posted

All –
  • Advanced Heart Failure

    Post Market Surveillance of the HeartMate 3 Left Ventricular Assist System in Korea

    • Completed
    • Age: 18 years and older
    • Medical device
    • Results posted

    The Korea HM3 PMS is a prospective, single arm, open-label, multi-center, post market surveillance is designed to evaluate clinical and functional outcomes with the HM3 LVAS as a treatment for advanced heart failure.

    Trial name
    NCT04915924
    Testing
    HeartMate 3™ left ventricular assist system (HM3 LVAS)
    Where
    22 sites in South Korea
    Volunteers
    358 people
    Sponsor
    Abbott Medical Devices
    Can I take part? NCT04915924
  • Chronic Pain

    CompaRison of Paresthesia Mapping to anatomIc Midline-based burSt Programming Strategies

    • Completed
    • Age: 18 years and older
    • Medical device
    • Results posted

    The study will compare therapeutic efficacy of a novel spinal cord stimulation leads implant based on anatomical landmarks with standard surgical implantation technique.

    Trial name
    CRISP (NCT02986074)
    Testing
    Paresthesia mapping lead evaluation first, Anatomical midline lead evaluation first
    Where
    2 sites in United Kingdom
    Volunteers
    60 people
    Sponsor
    Abbott Medical Devices
    Can I take part? CRISP
  • Cardiac Pacemaker, Artificial, Cardiac Rhythm Disorder

    Aveir DR i2i Study

    • Completed
    • Age: 18 years and older
    • Medical device
    • Results posted

    Prospective, non-randomized, multi-center, international study designed to evaluate the safety and effectiveness of the Aveir™ Dual-Chamber (DR) Leadless Pacemaker system.

    Conditions
    Cardiac Pacemaker, Artificial, Cardiac Rhythm Disorder, Bradycardia
    Trial name
    NCT05252702
    Testing
    Aveir DR Leadless Pacemaker System
    Where
    78 sites in United States, Austria and 11 more
    Volunteers
    464 people
    Sponsor
    Abbott Medical Devices
    Can I take part? NCT05252702
  • Cardiac Rhythm Disorder, Bradycardia

    The LEADLESS II IDE Study for the Aveir VR Leadless Pacemaker System

    • Completed
    • Age: 18 years and older
    • Medical device
    • Results posted

    prospective, non-randomized, multi-center, international clinical study is designed to confirm the safety and effectiveness of the Aveir LP System in a subject population indicated for a VVI(R) pacemaker.

    Trial name
    NCT04559945
    Testing
    Aveir VR Leadless Pacemaker System
    Where
    53 sites in United States, Canada and 6 more
    Volunteers
    1,276 people
    Sponsor
    Abbott Medical Devices
    Can I take part? NCT04559945
  • In-stent Restenosis

    CVT-ISR First in Human Trial for Coronary In-Stent Restenosis

    • Completed
    • Age: 18 years and older
    • Medical device
    • Results posted

    The goal of this first in human study is to assess the safety and inhibition of restenosis of the CVT Everolimus-coated PTCA Catheter in the treatment of subjects presenting in-stent restenotic lesions in native coronary arteries.

    Trial name
    NCT05731700
    Testing
    Drug Eluting Balloon
    Where
    9 sites in France, Georgia and 2 more
    Volunteers
    51 people
    Sponsor
    Abbott Medical Devices
    Can I take part? NCT05731700

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