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Multicenter Randomised Prospective Study for External Support Mesh VEST of Venous Coronary Grafts on the Right Territory (RiVEST)

C

Cardiochirurgia E.H.

Status

Enrolling

Conditions

Ischemic Cardiovascular Disease

Treatments

Procedure: CABG

Study type

Interventional

Funder types

Other

Identifiers

NCT06877195
MCRiVEST-1

Details and patient eligibility

About

Multicentre randomised prospective study aimed at verifying medium-term patency of venous grafts on the right coronary artery territory, by clinical and/or instrumental follow-up with particular attention to clinically driven re-revascularisation events regarding the site of new lesions (granularly comparing sites already treated with VEST, sites treated with bare vein, sites treated with other conduits, de novo lesions on the native).

Enrollment

300 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • combined or isolated interventions
  • adequate vein calibre
  • adequate graft flowmetry

Exclusion criteria

  • inability to implant due to calibre disparity or inadequate flowmetry

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

300 participants in 2 patient groups

Vested vein
Experimental group
Description:
Usage of External mesh support (VEST) around the venous graft
Treatment:
Procedure: CABG
Unvested vein
Active Comparator group
Description:
Normally harvested and preserved "naked" vein used as a graft
Treatment:
Procedure: CABG

Trial contacts and locations

1

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Central trial contact

Luca Paolo Weltert, MD

Data sourced from clinicaltrials.gov

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