AzTrials
AzTrials

Pharmaceutical sponsor

Boston Scientific Corporation Clinical Trials

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

537 registered studies

In numbers

Open to volunteers
39
Active
71
With results posted
285
All registered
537

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

Open to volunteers

All 39
  • Atrial Fibrillation (AF), Stroke Prevention in Patients With Atrial Fibrillation

    OPTION-EMEA Clinical Trial

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

    The OPTION-EMEA post-market study is intended to gather real world clinical data for patients undergoing AF ablation with the FARAPULSE™ Pulsed Field Ablation (PFA) System and subsequent left atrial appendage closure (LAAC) with…

    Conditions
    Atrial Fibrillation (AF), Stroke Prevention in Patients With Atrial Fibrillation, Left Atrial Appendage Closure, Pulsed Field Ablation
    Trial name
    OPTION-EMEA (NCT07349121)
    Testing
    Concomitant pulsed field ablation (PFA) and left atrial appendage closure (LAAC) during one interventional case, Concomitant Pulsed Field Ablation and Left Atrial Appendage Closure
    Where
    11 sites in Belgium, Croatia and 3 more
    Volunteers
    500 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? OPTION-EMEA
  • Weight Loss

    OverStitch NXT Endoscopic Suture System

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

    To demonstrate the safety and efficacy of OverStitch NXT Endoscopic Suture System for endoscopic sleeve gastroplasty(ESG) in obese populations to support the registration of OverStitch NXT for ESG indication.

    Trial name
    NCT07276815
    Testing
    OverStitch NXT Endoscopic Suture System
    Where
    China
    Volunteers
    136 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? NCT07276815
  • Weight Loss

    Orbera365 Intragastric Balloon System (Abbreviated as'Orbera365')

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

    To demonstrate the safety and efficacy of Orbera365 in obese populations to support the registration of Orbera365.

    Trial name
    NCT07195708
    Testing
    Treatment group
    Where
    China
    Volunteers
    144 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? NCT07195708
  • Acute Pulmonary Embolism

    A Real-World Study of EkoSonic Endovascular System in Chinese Populations With Acute Pulmonary Embolism

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

    This study to collect the real-world clinical outcome data of EkoSonicTM Endovascular System in Chinese patients with acute pulmonary embolism during practical clinical care.

    Trial name
    ANTEATER (NCT06819865)
    Testing
    EkoSonicTM Endovascular System
    Where
    China
    Volunteers
    30 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? ANTEATER
  • Persistent Atrial Fibrillation

    PVI Alone vs PVI and Linear Ablation for Persistent Atrial Fibrillation (PROMPT AF II)

    • Recruiting
    • Age: 18 to 80 years
    • Surgery or procedure

    This study is a prospective, multicenter, open-label, randomized controlled trial to investigate whether a linear ablation in addition to pulmonary vein isolation (PVI) outperforms PVI alone using pulsed field ablation (PFA) in…

    Trial name
    NCT07106970
    Testing
    Linear ablation, PVI alone
    Where
    China
    Volunteers
    640 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? NCT07106970
  • Type 2 Diabetes Mellitus (T2D), Obesity (BMI>30)

    Impact of Endoscopic Sleeve Gastroplasty (ESG) in Obese Adults With Type 2 Diabetes (T2D)

    • Not yet recruiting
    • Age: 22 years and older
    • Medical device

    The goal of this clinical trial is to determine whether Endoscopic Sleeve Gastroplasty (ESG)-induced weight loss can improve glycemic outcomes and alter the trajectory toward insulin dependence in adults with obesity and…

    Trial name
    MEASURE (NCT07639684)
    Testing
    ESG with OverStitch
    Volunteers
    50 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? MEASURE
  • Atrial Fibrillation, Persistent Atrial Fibrillation

    Feasibility Study of the FARAFLEX Mapping and PFA System

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

    The objective of this feasibility study is to evaluate the safety and effectiveness of the FARAFLEX mapping and pulsed field ablation (PFA) catheter, a novel catheter in treating persistent atrial fibrillation (PersAF) or…

    Conditions
    Atrial Fibrillation, Persistent Atrial Fibrillation, Paroxysmal AF
    Trial name
    ELEVATE-PF (NCT06510556)
    Testing
    FARAFLEX Ablation Treatment, ELEVATE-COR Sub-study
    Where
    4 sites in Belgium, Croatia and 2 more
    Volunteers
    250 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? ELEVATE-PF
  • Cardiac Arrythmias

    RHythmia mAPping and Signal acquisitiOn for Data analYsis (RHAPSODY)

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

    The objective of the RHAPSODY study is to evaluate the performance of new software features in subjects undergoing standard of care catheter-based endocardial mapping for atrial or ventricular tachyarrhythmias using a commercial…

    Trial name
    RHAPSODY (NCT03053141)
    Testing
    Rhythmia Mapping System
    Where
    8 sites in United States, Italy and 1 more
    Volunteers
    100 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? RHAPSODY
  • Paroxysmal Atrial Fibrillation, Persistent Atrial Fibrillation

    Evaluation of Novel Waveforms Delivered Using the FARAPULSE™ PFA System

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

    This is a multicenter, prospective, single-arm, feasibility study to evaluate the safety and effectiveness of the waveforms being delivered using the FARAPULSE PFA System in patients with Paroxysmal Atrial Fibrillation (PAF) and…

    Trial name
    IMPULSE-EVO (NCT07444320)
    Testing
    FARAPULSE™ Pulsed Field Ablation (PFA) System
    Where
    4 sites in Croatia, Czechia and 2 more
    Volunteers
    200 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? IMPULSE-EVO
  • Paroxysmal Atrial Fibrillation (PAF), Persistent Atrial Fibrillation

    Evaluation of the FARAFLEX Mapping and Pulsed Field Ablation System in Subjects With Atrial Fibrillation

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

    The goal of this clinical trial is to learn if the FARAFLEX™ Mapping and pulsed field ablation (PFA) System can safely and effectively treat symptomatic, drug-refractory Paroxysmal atrial fibrillation (PAF) and Persistent atrial…

    Trial name
    FARADIGM (NCT07575269)
    Testing
    FARAFLEX Mapping and Pulsed Field Ablation (PFA) System
    Where
    13 sites in United States, Belgium and 2 more
    Volunteers
    571 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? FARADIGM

Completed, with results posted

All 244
  • Parkinson Disease

    Closed Loop Programming Evaluation Using External Responses for Deep Brain Stimulation

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

    The objective of this study is to evaluate the performance of novel DBS programming methods compared to traditional programming methods.

    Trial name
    CLOVER (NCT03037398)
    Testing
    Vercise Deep Brain Stimulation System
    Where
    3 sites in Germany
    Volunteers
    69 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? CLOVER
  • ACC/AHA/NASPE Class 1, IIa or IIb Indications

    Subcutaneous Implantable Defibrillator (S-ICD) System - CE Clinical Investigation

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

    The primary objective is to evaluate the S-ICD system's ability to identify and terminate induced ventricular fibrillation in patients during the implant procedure.

    Trial name
    NCT01117792
    Testing
    subcutaneous implantable defibrillator (S-ICD) system
    Where
    8 sites in Italy, Netherlands and 2 more
    Volunteers
    55 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? NCT01117792
  • Coronary Artery Disease

    Safety and Effectiveness of Agent Paclitaxel-Coated PTCA Balloon Catheter. (AGENT Japan SV)

    • Completed
    • Age: 20 years and older
    • Medical device
    • Results posted

    A Randomized Trial Comparing the Agent Paclitaxel-Coated PTCA Balloon Catheter vs SeQuent Please Drug Eluting Balloon Catheter for the Treatment of a Small Vessel De Novo Native Coronary Artery Lesion.

    Trial name
    NCT04058990
    Testing
    Device: Paclitaxel-Coated PTCA Balloon Catheter, SeQuent Please Drug Eluting Balloon Catheter with Paclitaxel
    Where
    14 sites in Japan
    Volunteers
    180 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? NCT04058990
  • Coronary Artery Disease

    PROMUS PREMIER™ China Post-Approval Study

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

    To compile real-world clinical outcome data for the Promus PREMIERTM Everolimus-Eluting Platinum Chromium Coronary Stent System (Promus PREMIERTM Stent System) in routine clinical practice in China.

    Trial name
    NCT03273023
    Testing
    Promus PREMIERTM Everolimus-Eluting Platinum Chromium Coronary Stent System
    Where
    China
    Volunteers
    2,059 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? NCT03273023
  • Pain, Chronic

    Radiofrequency (RF) Ablation Prospective Outcomes Study

    • Completed
    • Age: 0 years and older
    • Observational study
    • Medical device
    • Results posted

    The objective of this study is to compile real-world outcomes of Boston Scientific commercially approved radiofrequency (RF) ablation systems in the treatment of patients diagnosed with pain

    Trial name
    RAPID (NCT04673032)
    Testing
    Radiofrequency Ablation
    Where
    15 sites in United States, Belgium and 2 more
    Volunteers
    298 people
    Sponsor
    Boston Scientific Corporation
    Can I take part? RAPID

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