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Pharmaceutical sponsor

W.L.Gore & Associates Clinical Trials

Studies where W.L.Gore & Associates is the lead sponsor: its pipeline by phase, what is enrolling now and where. Studies it supports as a collaborator are in the search.

96 registered studies

In numbers

Open to volunteers
21
Active
40
With results posted
57
All registered
96

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

Open to volunteers

All 21
  • Aortic Arch Dissection, Aortic Arch Aneurysm

    GORE® TAG® Thoracic Branch Endoprosthesis Zone 0/1 Post-Approval Study

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

    A prospective multi-center post-market study collecting outcomes through at least 5-years and up to 10-years post procedure for subjects treated with the TBE Device in Zone 0/1 as part of routine clinical practice.

    Trial name
    NCT07166133
    Testing
    GORE® TAG® Thoracic Branch Endoprosthesis
    Where
    22 sites in United States
    Volunteers
    125 people
    Sponsor
    W.L.Gore & Associates
    Can I take part? NCT07166133
  • Complex Aortic Aneurysms, Thoracoabdominal Aneurysm

    Real-World Data Collection of GORE Devices Used In the Endovascular Treatment of Aortic Aneurysms Which Incorporate Visceral Arteries.

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

    The registry population consists of patients presenting with complex aortic pathologies amenable to endovascular aortic repair that requires the incorporation of bridging stents to maintain visceral artery perfusion

    Conditions
    Complex Aortic Aneurysms, Thoracoabdominal Aneurysm, Fenestrated Endovascular Aortic Repair, Endovascular Aortic Repair
    Trial name
    ENVISION (NCT07480395)
    Where
    26 sites in Austria, Denmark and 8 more
    Volunteers
    400 people
    Sponsor
    W.L.Gore & Associates
    Can I take part? ENVISION
  • End Stage Renal Disease (ESRD), Kidney Failure

    A Study to Evaluate the Safety and Effectiveness of the InnAVasc Arteriovenous Graft for Hemodialysis Access in Patients With End-Stage Renal Disease

    • Recruiting
    • Age: 18 to 90 years
    • Medical device

    The goal of the CSP-2002 clinical trial is to evaluate the safety and effectiveness of the InnAVasc Arteriovenous Graft (IG) for hemodialysis (HD) access in patients with end-stage renal disease (ESRD).

    Conditions
    End Stage Renal Disease (ESRD), Kidney Failure, Chronic Renal Disease, Hemodialysis
    Trial name
    NCT04671771
    Testing
    InnAVasc Arteriovenous Graft (IG) surgical implant
    Where
    22 sites in United States
    Volunteers
    133 people
    Sponsor
    W.L.Gore & Associates
  • Ascites, Variceal Bleeding

    VIATORR® TIPS Study Evaluating 6-10mm Diameters (VIATIPS)

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

    This Registry will look at patients being treated with a transjugular intrahepatic portosystemic shunt (TIPS) procedure for portal hypertension.

    Conditions
    Ascites, Variceal Bleeding, Portal Hypertension Related to Cirrhosis
    Trial name
    VIATIPS (NCT07390344)
    Testing
    GORE® VIATORR® TIPS Endoprosthesis with Controlled Expansion (6-10mm)
    Where
    3 sites in United States
    Volunteers
    152 people
    Sponsor
    W.L.Gore & Associates
    Can I take part? VIATIPS
  • Thoracic Aortic Aneurysm, Penetrating Aortic Ulcers (PAUs)

    MBA Early Feasibility Study

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

    The MBA 25-04 study is a prospective, multicenter, non-randomized, single-arm, early feasibility study designed to assess the initial safety of the MBA device through five years following the index endovascular procedure.

    Conditions
    Thoracic Aortic Aneurysm, Penetrating Aortic Ulcers (PAUs), Thoracic Aortic Dissection, Pseudoaneurysm
    Trial name
    NCT07564375
    Testing
    GORE® Multibranch Arch Endoprosthesis, GORE® Ascending Stent Graft
    Where
    3 sites in United States
    Volunteers
    20 people
    Sponsor
    W.L.Gore & Associates
  • Vascular Disease, Dissection

    Long-term Characterization of GORE® TAG® Conformable Thoracic Stent Graft With ACTIVE CONTROL System Performance

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

    An observational, prospective multi-regional post-market registry collecting mid- and long-term data to assess outcomes through ten years of follow-up for subjects treated with GORE® TAG® Conformable Thoracic Stent Graft with…

    Conditions
    Vascular Disease, Dissection, Dissection Aortic Aneurysm, Dissection of Aorta
    Trial name
    TGR 23-02TA (NCT06658730)
    Testing
    Endovascular
    Where
    37 sites in United States, Denmark and 8 more
    Volunteers
    1,500 people
    Sponsor
    W.L.Gore & Associates
    Can I take part? TGR 23-02TA
  • Chronic Kidney Diseases, End Stage Renal Disease on Dialysis

    Registry of GORE® ACUSEAL Vascular Graft in Dialysis Access

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

    The goal of this observational study is to evaluate safety and performance of GORE® ACUSEAL Vascular Graft for the treatment of CKD in patients with ESRD in hemodialysis.

    Trial name
    AVG22-09 (NCT05846581)
    Testing
    GORE® ACUSEAL Vascular Graft
    Where
    4 sites in Germany, Italy and 1 more
    Volunteers
    72 people
    Sponsor
    W.L.Gore & Associates
    Can I take part? AVG22-09
  • Venous Thromboses, Venous Disease

    The GORE® VIABAHN® FORTEGRA Venous Stent Post-Approval Study

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

    This study is a prospective, multicenter, single-arm post-market clinical study to evaluate the GORE® VIABAHN® FORTEGRA Venous Stent in real-world use.

    Conditions
    Venous Thromboses, Venous Disease, Venous Leg Ulcer, Venous Stasis
    Trial name
    NCT07538609
    Testing
    GORE® VIABAHN® FORTEGRA Venous Stent
    Volunteers
    150 people
    Sponsor
    W.L.Gore & Associates
    Can I take part? NCT07538609
  • Dissection of Aorta, Aneurysm Aortic

    Retrospective Real-World Data Collection of the Conformable GORE® TAG® Thoracic Endoprosthesis When Used in Frozen Elephant Trunk Procedures for Treatment of Aortic Aneurysms and Dissections

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

    Retrospective, multicenter, single-arm registry data collection designed to characterize outcomes in patients treated with the Conformable GORE® TAG® Thoracic Endoprosthesis deployed in an antegrade fashion as part of a frozen…

    Conditions
    Dissection of Aorta, Aneurysm Aortic, Frozen Elephant Trunk
    Trial name
    NCT07742592
    Testing
    Antegrade deployment of covered thoracic aortic stent graft as completion in frozen elephant trunk procedure
    Volunteers
    350 people
    Sponsor
    W.L.Gore & Associates
  • Stroke, PFO - Patent Foramen Ovale

    GORE® CARDIOFORM Septal Occluder and Antiplatelet Medical Management for Reduction of Recurrent Stroke in Patients With Patent Foramen Ovale (PFO): the REDUCE Post Approval Study

    • Recruiting
    • Age: 18 to 70 years
    • Medical device

    This study will assess the safety and effectiveness of GORE® CARDIOFORM Septal Occluder in a post approval setting and evaluate the quality of operator education and training and transferability of trial experience to a…

    Trial name
    REDUCE PAS (NCT03821129)
    Testing
    PFO closure with GORE® CARDIOFORM Septal Occluder
    Where
    45 sites in United States
    Volunteers
    636 people
    Sponsor
    W.L.Gore & Associates
    Can I take part? REDUCE PAS

Completed, with results posted

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