| Detected | Trial | Change |
|---|---|---|
| 2026-06-11 | NCT06526195 Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in Patients… |
Trial sites expanded: 63 -> 68 locations |
| 2026-06-03 | NCT07361445 Agilis RF TSP Early Feasibility Study |
Enrollment increased: 20 -> 60 participants |
| 2026-06-02 | NCT06676072 A Study of the TactiFlex SE Catheter and Volt PFA Generator in Subjects With PAF: |
Trial completed |
| 2026-05-28 | NCT07523620 Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration |
overall status: "Withheld" → "Recruiting" |
| 2026-05-28 | NCT07523620 Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration |
Phase changed: [] -> ['NA'] |
| 2026-05-28 | NCT07523620 Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration |
Primary endpoint(s) modified |
| 2026-05-28 | NCT07523620 Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration |
Enrollment changed: None -> 240 |
| 2026-05-28 | NCT07523620 Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration |
Sponsor changed: [Redacted] -> Abbott Medical Devices |
| 2026-05-28 | NCT07523620 Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration |
Trial arms changed: 0 -> 1 |
| 2026-05-28 | NCT07523620 Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration |
Trial sites expanded: 0 -> 13 locations |
| 2026-05-23 | NCT06423430 Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND) |
Trial sites reduced: 28 -> 24 locations |
| First Posted | Trial | Phase | Status |
|---|---|---|---|
| 2026-05-14 | NCT07586995 A Post-Market Assessment of the Safety and Performance of the TriClip™ System | Enrolling by Invitation |
| NCT ID | Title | Condition | Status |
|---|---|---|---|
| Not specified | |||
| NCT03876054 | Long-Term Real-World Outcomes Study on Patients Implanted With a Neurostimulator | Chronic Pain | Recruiting |
| NCT04071847 | Abbott DBS Post-Market Study of Outcomes for Indications Over Time | Movement Disorders | Recruiting |
| NCT07244939 | Cephea South America Feasibility Study | Mitral Regurgitation | Recruiting |
| NCT06779552 | CardioMEMS HF System Coverage With Evidence Development Study | Heart Failure | Recruiting |
| NCT07509658 | TriClip Japan Post-Approval Study | Tricuspid Regurgitation | Recruiting |
| NCT07373353 | A Clinical Evaluation of AMJ-401 | Ischemic Heart Disease (IHD) | Recruiting |
| NCT05061004 | Cephea Early Feasibility Study | Mitral Regurgitation | Recruiting |
| NCT04754217 | Valved Graft PMCF Study | Aortic Valve Disease | Recruiting |
| NCT06590467 | Abbott Structural Heart Device Registry | Heart Diseases | Recruiting |
| NCT07217392 | Left Bundle Branch Area Pacing (LBBAP) PMCF Study | Bradycardia | Recruiting |
| NCT07421076 | Grid eXplore Mapping Study | Paroxysmal Atrial Fibrillation (PAF) | Recruiting |
| NCT07069673 | Abbott Cephea Mitral Valve Disease Registry | Mitral Regurgitation | Recruiting |
| NCT07106788 | Aveir Leadless Pacemaker Japan PMS | Leadless Pacemaker | Recruiting |
| NCT04761120 | Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study | Mitral Regurgitation | Recruiting |
| NCT05935007 | Aveir DR Real-World Evidence Post-Approval Study | Cardiac Pacemaker | Recruiting |
| NCT07181590 | BaLloon-based PFA Ablation poST Approval Outcomes for PAF and PersAF | Paroxysmal AF | Recruiting |
| NCT07193888 | Navitor Japan Study | Severe Aortic Stenosis | Recruiting |
| NCT07523620 | Comprehensive LEFt Atrial Appendage Occlusion With Rhythm Restoration | Atrial Fibrillation (AF) | Recruiting |
| NCT06772493 | ViewFlex X ICE First-in-Human Study | Cardiac Arrhythmias | Recruiting |
| NCT07361445 | Agilis RF TSP Early Feasibility Study | Cardiac Arrythmias | Recruiting |
| NCT06423430 | Treatment ResistAnt Depression Subcallosal CingulatE Network DBS (TRANSCEND) | Treatment Resistant Depression | Recruiting |
| NCT06526195 | Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in Patients… | Heart Failure | Recruiting |
| NCT04227899 | LIFE-BTK Randomized Controlled Trial | Critical Limb Ischemia (CLI) | Active, Not Recruiting |
| NCT05208905 | LIFE-BTK PK Sub-study | Critical Limb Ischemia (CLI) | Active, Not Recruiting |
| NCT07116551 | Early Feasibility Study (EFS) of Abbott's Balloon-expandable (BE) TAVI System for the… | Symptomatic Severe Aortic Stenosis | Active, Not Recruiting |