Viewing Study NCT00139399



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Last Modification Date: 2024-10-26 @ 9:14 AM
Study NCT ID: NCT00139399
Status: COMPLETED
Last Update Posted: 2019-06-25
First Post: 2005-08-30

Brief Title: Radial Artery Versus Saphenous Vein Patency RSVP Study
Sponsor: Imperial College London
Organization: Imperial College London

Study Overview

Official Title: A Randomised Controlled Trial to Compare Angiographic Patency of Radial Artery Versus Saphenous Vein Used as Free Aorto-coronary Grafts in Coronary Revascularization
Status: COMPLETED
Status Verified Date: 2019-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: RSVP
Brief Summary: The purpose of this study is to determine whether the radial artery artery in the arm or saphenous vein vein in the leg when used as bypass grafts for coronary artery bypass surgery have a greater patency rate degree of openingat 5 years after surgery
Detailed Description: Arteries differ from veins both in morphology and physiology Thus the way they behave as in vivo conduits when used in coronary artery bypass grafting is also likely to be different This may partly explain the predisposition of veins used as coronary conduits to accelerated atherosclerosis in comparison with the internal mammary artery grafts There are presently few data describing the properties of the radial artery as an in-vivo coronary conduit over the longer-term

The study will compare angiographic patency of the radial artery or saphenous vein graft anastomosed to the native left circumflex coronary territory at 3 months and 5 years after surgery A substudy will compare 5-year post-surgery diameter and blood flow of in-vivo radial artery and saphenous vein grafts in response to endothelium-dependent and non-endothelium-dependent stimuli when patients attend for their scheduled follow-up angiogram

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None