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 5 of 6
PLATINUM Trial to Assess the PROMUS Element Stent System for Treatment of De Novo Coronary Artery Lesions-Pharmacokinetics (PLATINUM PK)
NCT01510327
Multicenter Automatic Defibrillator Implantation Trial - Reduce Inappropriate Therapy
NCT00947310
Longitudinal Surveillance Registry (LSR) of ACUITY Spiral
NCT00955708
An Open-label, Single-dose Pilot Study to Evaluate Varisolve® (Polidocanol Endovenous Microfoam (PEM)) 0.125% [0.2%] for Varicose Veins
NCT00928421
EPIC Nitinol Stent System in the Treatment of Atherosclerotic Lesions in Iliac Arteries
NCT00896337
Optimized Programming in Spinal Cord Stimulation (SCS) System
NCT00871819
The PLATINUM Clinical Trial to Assess the PROMUS Element Stent System for Treatment of De Novo Coronary Artery Lesions in Small Vessels
NCT01498692
The PLATINUM Clinical Trial to Assess the PROMUS Element Stent System for Treatment of Long De Novo Coronary Artery Lesions (PLATINUM LL)
NCT01500434
The PLATINUM Clinical Trial to Assess the PROMUS Element Stent System for Treatment of De Novo Coronary Artery Lesions
NCT00823212
Evaluation of Left Ventricular AutoThreshold
NCT00812201
A Carotid Stenting Boston Scientific Surveillance Program
NCT00741091
APPROPRIATE - Rate Adaptive Pacing Sensor
NCT00757666
Correlation Of Respiratory Rate Level And Trend Evaluation in Heart Failure Patients
NCT00758121
Randomized, Single Blind, Placebo Controlled, to Evaluate Efficacy and Safety of Polidocanol Injectable Foam for Treatment of Symptomatic, Visible Varicose Veins With SFJ Incompetence
NCT00758420
Restoration of Chronotropic Competence in Heart Failure Patients With Normal Ejection Fraction
NCT00670111
Investigating Superion™ In Spinal Stenosis
NCT00692276
Comparison of AV Optimization Methods Used in Cardiac Resynchronization Therapy (CRT)
NCT00677014
Efficacy and Safety of OncoGel™ Added to Chemotherapy and Radiation Before Surgery in Subjects With Esophageal Cancer
NCT00573131
A Study Evaluating the Safety and Efficacy of BGC20-0582 Lice Treatment Gel for Head Lice Infestation
NCT00528021
TAXUS PERSEUS Workhorse
NCT00484315
TAXUS PERSEUS Small Vessel
NCT00489541
Post-Approval Study of the NexStent Carotid Stent System and the FilterWire EZ Embolic Protection System: SONOMA
NCT00478673
A Study of the WallFlex™ Biliary Fully-covered Stent for the Palliative Treatment of Malignant Bile Duct Obstruction
NCT00433771
Safety Study of Varisolve® Procedure for Treatment of Varicose Veins in Patients With Right-to-left Cardiac Shunt
NCT00442364
A Phase 1 / 2 Dose Escalation Study of Locally-Administered OncoGel™ in Subjects With Recurrent Glioma
NCT00479765
Spinal Cord Stimulation for Painful Diabetic Neuropathy
NCT00487981
Changes in Cerebral Blood Flow in Patients Treated With Spinal Cord Stimulation for Low Back and Leg Pain
NCT00418301
TheraSphere for the Treatment of Liver Metastases
NCT00511862
The Prefyx PPS™ System eRegistry
NCT00688181
Spy II Clinical Registry
NCT00751998
Effect of Pulse Width With Spinal Cord Stimulation
NCT00399516
Spinal Cord Stimulation (SCS) for Neuropathic Pain of Back or Lower Extremity
NCT00399841
Effectiveness of Precision Spinal Cord Stimulation With Artisan Paddle Electrode
NCT00386724
Efficacy of the Spinal Cord Stimulation System as Salvage Therapy
NCT00387244
TC-WYRE: TAXUS Express Stent vs. Cypher Stent - What's Your Real Life Experience?
NCT00344630
RAPID-RF: Remote Active Monitoring in Patients With Heart Failure
NCT00334451
REASSURE AV Registry
NCT01074034
EASYTRAK 3 Downsize Lead
NCT00384722
Treatment for Migraines With an Implantable Device
NCT00286078
Spinal Cord Stimulation for Chronic and Intractable Back Pain
NCT00370695
A Prospective Study Comparing Contour SE™ Microspheres to Embosphere® Microspheres for Treating Symptomatic Uterine Fibroids With Uterine Fibroid Embolization (UFE)
NCT00628901
Comparison of Intraspinal Nerve Root Stimulation With Dorsal Column Stimulation
NCT00370773
First Arrhythmia Collection of Transvenous and Simultaneous Subcutaneous Implantable Defibrillator Data
NCT01161589
Asthma Intervention Research 2 (AIR2) Trial
NCT00231114
ULTRA Study for Pacemaker Patients
NCT00133289
RIGHT: Rhythm ID Going Head-to-Head Trial
NCT00148954
Guidant Microwave Ablation System for the Treatment of Atrial Fibrillation
NCT00111488
The Prevention of Myocardial Enlargement and Dilatation Post Myocardial Infarction Study
NCT00605631
EASYTRAK 4 Steerable LV Lead
NCT00158964
Direct Stenting of TAXUS Liberté™-SR Stent for the Treatment of Patients With de Novo Coronary Artery Lesions
NCT00371423
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.