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A prospective study to assess the screening value of N-terminal pro-B-type natriuretic peptide (NT-proBNP) for the identification of patients that benefit from additional cardiac testing prior to vascular surgery.

Recruiting
Conditions
Perioperative cardiac risk stratification
10011082
10003184
Registration Number
NL-OMON30697
Lead Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
1000
Inclusion Criteria

Patients with peripheral vascular atherosclerosis scheduled for vascular surgery involving either; a) revascularization utilizing aortic or proximal lower extremity procedures, or b) distal lower extremity vascular reconstruction, are eligible to participate.

Exclusion Criteria

No written informed consent.
Unstable coronary disease.
Undergoing emergency surgery.
Previous participation in the DECREASE VI trial.
Reoperation within 30 days of an initial surgical procedure.
Participation in another clinical trial within the last 30 days.
Age <18 years

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary objective of this trial is to validate the screening potential of<br /><br>NT-proBNP in a population of low to intermediate risk patients, i.e. patients<br /><br>with zero to two cardiac risk factors, scheduled for vascular surgery.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>The secondary objective is to identify prior to vascular surgery high risk<br /><br>patients, with three or more cardiac risk factors, with a normal stress test.</p><br>
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