Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02790606 · ClinicalTrials.gov registry record · NA

Clinical Study of the BARD® COVERA™ Arteriovenous (AV) Stent Graft in AV Graft Patients (AVeVA)

A NA study, sponsored by C. R. Bard.

Completed
Registry status
NA
Development phase
110
Enrollment target

NCT02790606: Completed NA study, sponsored by C. R. Bard.

NCT02790606 is a NA study that has completed, run by C. R. Bard. The registered enrollment target is 110 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02790606, a NA study, has completed, sponsored by C. R. Bard.

COMPLETED
Registry status
NA
Development phase
110 participants
Enrollment target

Study Summary

The objective of this study is to assess the safety and effectiveness of the COVERA™ Vascular Covered Stent for the treatment of stenotic lesions in the upper extremity venous outflow of the Arteriovenous (AV) access circuit.

Primary Outcome

Safety is defined as freedom from any adverse event(s) (AEs), localized or systemic, that reasonably suggests the involvement of the AV access circuit (not including stenosis or thrombosis) that require or result in any of the following alone or in combination: additional interventions (including surgery); in-patient hospitalization or prolongation of an existing hospitalization; or death.

Interventions

  • DEVICE Covera(TM) Vascular Covered Stent

Trial Details

FieldValue
Enrollment Target 110 participants
Start Date 2016-07
Est. Completion 2019-03-16
Phase NA
C. R. Bard

75 total trials

What the finished NCT02790606 record still lists

NCT02790606 is an interventional study that assigns participants to a tested intervention. The registered 110 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which Covera(TM) Vascular Covered Stent is the first listed.

NCT02790606 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02790606 about?

NCT02790606 is a clinical study titled "Clinical Study of the BARD® COVERA™ Arteriovenous (AV) Stent Graft in AV Graft Patients (AVeVA)". The objective of this study is to assess the safety and effectiveness of the COVERA™ Vascular Covered Stent for the treatment of stenotic lesions in the upper extremity venous outflow of the Arteriovenous (AV) access circuit.

What is the current status of trial NCT02790606?

This trial is currently completed. It is a NA study. The enrollment target is 110 participants. The study started on 2016-07. Estimated completion is 2019-03-16.

What interventions are being tested in trial NCT02790606?

The interventions under investigation include: Covera(TM) Vascular Covered Stent (DEVICE).

Who is sponsoring clinical trial NCT02790606?

This trial is sponsored by C. R. Bard, which has 75 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02790606's enrollment target sits among peer trials

110 816th of 2000 higher than 1,176 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01530373 · 110 participants · Phase 2

    Solifenacin Compared to Clonidine for Reducing Hot Flashes Among Breast Cancer Patients

  • NCT02379377 · 110 participants · Phase 1

    18F-FSPG PET in Imaging Patients With Liver Cancer Before Undergoing Surgery or Transplant

  • NCT02411773 · 110 participants · Phase 1

    Sympatholysis in Chronic Kidney Disease

  • NCT03190941 · 110 participants · Phase 1

    Administering Peripheral Blood Lymphocytes Transduced With a Murine T-Cell Receptor Recognizing the G12V Variant of Mutated RAS in HLA-A*11:01 Patients

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02790606, the US trial registry maintained by the National Library of Medicine. NCT02790606 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.