Boston Scientific Corporation
Boston Scientific Corporation sponsors 280 registered US clinical trials on ClinicalTrials.gov, 22 of them currently recruiting, and 207 completed. 59 of these trials are in Phase 3-4 (later-stage) and 23 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Coronary Artery Disease, with 8 trials.
Trial Pipeline
280 total, page 1 of 6
Evaluation of the FARAFLEX Mapping and Pulsed Field Ablation System in Subjects With Atrial Fibrillation
NCT07575269
Fainting Detection And Early Warning In Syncope Evaluation Study (ARISE)
NCT07502599
Respiration Measured Via End-tidal CO2 and Spirometry Study (RESPI)
NCT07537478
Five PLus Year EffIcacy of Endoscopic Sleeve Gastroplasty (ESG) for Sustained WeigHT Loss
NCT06894498
Endo-SPONGE for Treatment of Anastomotic or Hartmann's Stump Leakages in Lower Pelvic Area
NCT07035431
Randomized Study on Transoral Outlet Reduction and Lifestyle Changes for Weight Regain After Gastric Bypass
NCT07015424
RESCUE: Discontinuation of GLP-1
NCT07190794
A Global Study Comparing Pulsed Field Ablation With Electrographic Flow Mapping Versus Posterior Wall Ablation for Persistent Atrial Fibrillation
NCT07187115
Managing Pain Using Optimized Sequences by Adjusting Parameters With Independent Current Control
NCT07190807
Safety and Effectiveness of Left Bundle Branch Area Pacing Versus Conventional Cardiac Resynchronization Therapy in Heart Failure
NCT07069738
AGENT DCB STANCE: Safety and Effectiveness Study of AGENT Drug-Coated Balloon Compared to Standard of Care Percutaneous Coronary Intervention (PCI) Treatment for de Novo Coronary Lesions
NCT06959524
Stone and Laser Therapies Post-Market Study (SALT)
NCT06982235
Repeat Ablation of Persistent Atrial Fibrillation, Including Mitral Isthmus Catheter Ablation, With the FARAPULSE Pulsed Field Ablation System
NCT06735534
Intracept Minimally-invasive PROcedure for VErtebrogenic Back Pain
NCT06827262
POLARx Post Approval Study (POLARx PAS)
NCT06170606
A DirEct to PatieNt Study in Chronic Pain
NCT05515341
A Feasibility Study to Evaluate the Safety of the TheraSphere Glioblastoma (GBM) Device in Patients With Recurrent GBM
NCT05303467
Drug-Eluting Registry: Real-World Treatment of Lesions in the Peripheral Vasculature
NCT04674969
Deep Brain Stimulation (DBS) Retrospective Outcomes Study
NCT03664609
Registry of Deep Brain Stimulation With the VERCISE™ System: Vercise DBS Registry
NCT02071134
RELIEF - A Global Prospective Observational Post-Market Study to Evaluate Long-Term Effectiveness of Neurostimulation Therapy for Pain
NCT01719055
Patient Retrospective Outcomes (PRO)
NCT01550575
SpaceIT Hydrogel System for Perirectal Spacing
NCT06451614
A Clinical Trial to Assess the Agent Paclitaxel Coated PTCA Balloon Catheter for the Treatment of Subjects With In-Stent Restenosis (ISR) - Long Lesion Cohort
NCT06492174
SIMPLAAFY Clinical Trial
NCT06521463
ADVENT Post Approval Study
NCT06431815
Dose Escalation Study Evaluating Safety of TheraSphere Prostate Cancer (PCa) Device
NCT06192758
Pulsed Field Ablation (PFA) vs Anti-Arrhythmic Drug (AAD) Therapy as a First Line Treatment for Persistent Atrial Fibrillation
NCT06096337
TheraSphere With Durvalumab and Tremelimumab for HCC
NCT05063565
Effectiveness of the SpaceOAR Vue System in Subjects With Prostate Cancer
NCT04905069
Ultrasound-facilitated, Catheter-directed, Thrombolysis in Intermediate-high Risk Pulmonary Embolism
NCT04790370
Effectiveness of the EMPOWER™ Modular Pacing System and EMBLEM™ Subcutaneous ICD to Communicate Antitachycardia Pacing
NCT04798768
A Clinical Trial to Assess the Agent Paclitaxel Coated PTCA Balloon Catheter for the Treatment of Subjects With In-Stent Restenosis (ISR)
NCT04647253
LUX-Dx TRENDS Evaluates Diagnostics Sensors in Heart Failure Patients Receiving Boston Scientific's Investigational ICM System.
NCT04790344
Paresthesia-Free Fast-Acting Subperception (FAST) Study
NCT04618471
CHAMPION-AF Clinical Trial
NCT04394546
A 5-year Superion™ IDS Clinical Outcomes Post-Approval Evaluation (SCOPE)
NCT04192591
A Feasibility Study of the Millipede Transcatheter Annuloplasty Ring System in Patients With Functional Mitral Regurgitation
NCT04147884
ACURATE IDE: Safety and Effectiveness Study of ACURATE Valve for Transcatheter Aortic Valve Replacement
NCT03735667
Intra-operative Pancreatoscopy in Patients With IPMN
NCT03729453
RHythmia mAPping and Signal acquisitiOn for Data analYsis (RHAPSODY)
NCT03053141
ADVENT Trial Long Term Outcomes Evaluating Atrial Fibrillation Progression Study
NCT06526546
Obsidio™ Conformable Embolic Registry
NCT06170619
VITALYST Early Feasibility Study in High-Risk PCI Patients (VITALYST EFS)
NCT06132568
SpyGlass Surgical Study
NCT05822635
HEAL-LAA Clinical Trial
NCT05809596
MANTIS Endoscopic Clipping Study
NCT05653843
A Prospective Single Arm Open Label Study of the FARAPULSE Pulsed Field Ablation System in Subjects With Persistent Atrial Fibrillation
NCT05443594
Varithena Versus Endothermal Ablation of the Great Saphenous Vein (VERITAS)
NCT05312970
TheraSphere Post-Approval Study to Calculate the Radiation-absorbed Dose of Tc-99m MAA.
NCT05233098
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 7 |
| Phase 2 | 16 |
| Phase 3 | 33 |
| Phase 4 | 26 |
Therapeutic Areas
What the Pipeline for Boston Scientific Corporation Shows
According to the ClinicalTrials.gov registry, Boston Scientific Corporation is linked to 280 US clinical trials across every stage of research activity. Of those, 22 studies are currently recruiting, about 8% of the sponsor's indexed portfolio, and 207 are already marked complete, representing roughly 74% of the total.
The phase mix for Boston Scientific Corporation reports 59 late-stage studies (Phase 3 and Phase 4 combined) and 23 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Boston Scientific Corporation is Coronary Artery Disease with 8 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.