The eSVS (TM) Mesh External Saphenous Vein Support Trial

NCT00777777 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2008-10-22

No results posted yet for this study

Summary

Prospective, multi-center, randomized, controlled (patients as their own control) trial on an external mesh device (eSVS™, Kips Bay Medical) supporting saphenous vein grafts for coronary bypass graft surgery in patients with multi-vessel coronary heart disease.

Conditions

Interventions

DEVICE

eSVS, saphenous vein supporting mesh

Surgical coronary artery bypass grafting to the right coronary artery and the circumflex coronary artery with saphenous vein grafts, one will be supported by the eSVS(TM).

Sponsors & Collaborators

  • Kips Bay Medical, Inc.

    collaborator INDUSTRY
  • Transmedic Pte Ltd, Singapore

    collaborator UNKNOWN
  • National University Hospital, Singapore

    lead OTHER

Principal Investigators

  • Uwe Klima, MD, PhD · Department of Cardiac, Thoracic and Vascular Surgery, National University Hospital Singapore

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-08-31
Primary Completion
2009-06-30
Completion
2009-09-30

Countries

  • Singapore

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00777777 on ClinicalTrials.gov