Example: Heart Attack

Clinical Trials Sponsored by C. R. Bard

Total 95 results

    • NCT04634916
      Not yet recruiting
      Post-market Surveillance Study of the BD® WavelinQ™ EndoAVF System
      Conditions: Kidney Disease, End-Stage; End-stage Renal Disease; Arteriovenous Fistula
    • NCT04626427
      Recruiting
      The WavelinQ™ Arterio-Venous Endovascular Fistula: A Global, Post-Market Investigation
      Conditions: End Stage Kidney Disease; Chronic Kidney Diseases; Kidney Failure; Kidney Insufficiency; Kidney Disease, Chronic; AV Fistula; Fistulas Arteriovenous
    • NCT04261686
      Enrolling by invitation
      Post Approval Study of the BARD® COVERA™ Arteriovenous (AV) Stent Graft
      Conditions: Arteriovenous Fistula
    • NCT04244370
      Recruiting
      Caterpillar™ Arterial Embolization Device Post-Market Study
      Conditions: Embolization, Therapeutic
    • NCT04090320
      Completed
      CATERPILLAR™ Arterial Embolization Device Study
      Conditions: Embolization, Therapeutic
    • NCT03506308
      Recruiting
      Post Approval Study Investigating Lutonix Drug Coated Balloon for Treatment of Dysfunctional Arteriovenous Fistulae
      Conditions: Arteriovenous Fistula
    • NCT03288766
      Recruiting
      SHERLOCK 3CG™ Diamond Tip Confirmation System
      Conditions: Indication for Peripheral Intravenous Catheterization; Atrial Flutter; Premature Atrial Contraction; Premature Ventricular Contraction; Premature Junctional Contraction; Tachycardia; Atrioventricular Block; Bundle-Branch Block
    • NCT03193619
      Enrolling by invitation
      Real World Registry Assessing the Clinical Use of the Bard UltraScore Forced Focus PTA Balloon
      Conditions: Peripheral Arterial Disease; Peripheral Vascular Diseases; Arterial Occlusive Diseases
    • NCT03071146
      Completed
      Utility, Safety, and Effectiveness of the Bard LifeStent 5F Vascular Stent System
      Conditions: Peripheral Arterial Disease; Intermittent Claudication
    • NCT03028090
      Completed
      Study to Assess Electrocardiogram Waveforms Produced Through the Utilization of the Sherlock 3CG™ Tip Confirmation System
      Conditions: Indication for Peripheral Intravenous Catheterization
    • NCT02996266
      Recruiting
      Impact of Fever Prevention in Brain Injured Patients
      Conditions: Fever; Ischemic Stroke; Intracerebral Hemorrhage; Subarachnoid Hemorrhage
    • NCT02847546
      Completed
      Evaluation of the BARD® True™ Flow Valvuloplasty Perfusion Catheter for Aortic Valve Dilatation
      Conditions: Aortic Valve Stenosis
    • NCT02813577
      Terminated
      Lutonix Drug Coated Balloon for Treatment of Femoropopliteal Arteries in United States Females (CONFIRM)
      Conditions: Femoral Artery Stenosis; Popliteal Artery Stenosis; Femoral Artery Occlusion; Popliteal Artery Occlusion
    • NCT02792764
      Completed
      Post-Marketing Study to Assess Complication Rates of Oncology Patients With Ports and Peripheral IVs
      Conditions: PORTs/Peripheral IVs Complication Rates
    • NCT02790606
      Completed
      Clinical Study of the BARD® COVERA™ Arteriovenous (AV) Stent Graft in AV Graft Patients (AVeVA)
      Conditions: Stenosis; Restenosis
    • NCT02746159
      Completed
      Lutonix® Global AV Registry
      Conditions: Arteriovenous Fistula
    • NCT02720042
      Completed
      Study of Phasix™ Mesh for VHWG Grade 3 Midline Hernia Repair
      Conditions: Hernia; Hernia, Abdominal; Hernia, Incisional
    • NCT02720003
      Completed
      A Single Arm Trial Evaluating the BARD Lutonix Drug-Coated Balloon (LTX DCB) for Treatment of Femoropopliteal Arteries
      Conditions: Femoral Artery Stenosis; Femoral Artery Occlusion; Stenosis of Popliteal Arteries; Occlusion of Popliteal Arteries
    • NCT02717104
      Completed
      Korean Post-market Registry Assessing the Clinical Use and Safety of the Lutonix DCB in Femoropopliteal Arteries
      Conditions: Peripheral Artery Disease
    • NCT02712398
      Completed
      A Prospective Trial of a Bio-absorbable Mesh in Challenging Laparoscopic Ventral or Incisional Hernia Repair
      Conditions: Hernia, Ventral; Incisional Hernia
    • NCT01870401
      Active, not recruiting
      Lutonix DCB Versus Standard Balloon Angioplasty for Treatment of Below-The-Knee (BTK) Arteries
      Conditions: Critical Limb Ischemia
    • NCT02691962
      Completed
      Xen Matrix™ AB Surgical Graft in Ventral or Incisional Midline Hernias
      Conditions: Incisional Hernia
    • NCT01864278
      Completed
      Lutonix Global SFA Registry
      Conditions: Peripheral Artery Disease
    • NCT02655887
      Active, not recruiting
      BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease
      Conditions: May-Thurner Syndrome; Peripheral Vascular Disease; Venous Disease; Iliofemoral Occlusive Disease
    • NCT02649946
      Active, not recruiting
      Clinical Study of the BARD® COVERA™ Arteriovenous (AV) Stent Graft
      Conditions: Stenosis; Restenosis
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