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Randomized Evaluation of Vascular Entry Site and Radiation Exposure: REVERE Trial

T

Total Cardiovascular Solutions

Status

Completed

Conditions

Exposure to Ionizing Radiation

Study type

Observational

Funder types

Other

Identifiers

NCT01677481
MIL/IMRC/RP/TP/10/2010

Details and patient eligibility

About

The study compares radiation exposure parameters between coronary angiography procedures performed by left wrist, right wrist or groin (femoral) procedure access site

Full description

Patients referred for coronary angiography will be randomized to either left radial, right radial or femoral arterial access sites, and the coronary angiogram will be performed in a standard fashion, including left ventriculography. Radiation exposure parameters including Air Kerma, Dose-area product, Fluoroscopy time and Operator radiation exposure will be recorded. Operator experience as well as demographic data will be recorded.

Enrollment

1,500 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients undergoing diagnostic coronary angiography

Exclusion criteria

  • non-availability of one or more of the three access sites History of coronary artery bypass graft surgery Need for percutaneous coronary intervention.

Trial design

1,500 participants in 3 patient groups

Femoral
Description:
Coronary angiography procedures performed using transfemoral access
Left radial access
Description:
Coronary angiography procedures performed using left radial access site.
Right radial Access
Description:
Coronary angiography procedures performed using Right radial access site.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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