Skip to content

A study to determine the ability of a blood test for B-type Natriuretic Peptide signal peptide (BNP-SP) to act as an early indicator in Acute Coronary Syndrome (ACS)).

A study to determine the diagnostic test performance (sensitivity, specificity, negative predictive value, positive predictive value, accuracy and prognostic value) of B-type Natriuretic Peptide Single Peptide (BNP-SP) measurement in detection of Acute Coronary Syndrome (ACS) (including those with ischemia short of infarction) within a population of “all-comers” with chest discomfort Signal Peptide in Acute Coronary Events

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12609000057280
Acronym
The Signal Peptide in Acute Coronary Events Study: "SP-ACE"
Enrollment
1255
Registered
2009-01-23
Start date
2007-11-16
Completion date
2030-12-31
Last updated
2026-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Early clinical detection of acute coronary syndromes (ACS) can be difficult. In particular, distinction between cardiac and non-cardiac events may entail 12-36 hours of delay whilst serial biomarker results are awaited and/or subsequent tests (such as exercise electrocardiography) are performed. We have achieved the first ever identification of a signal peptide in the circulation (B-type Natriuretic Peptide signal peptide (BNP-SP)) and show that it has potential to specifically and rapidly identify cardiac ischemia.. We will measure serial BNP-SP concentrations in 2000 patients presenting to the Emergency Department within 24 hours of symptom onset of possible Acute Coronary Syndrome (ACS). Clinical history and physical examination will be undertaken according to standard care . Venous blood samples for cardiac biomarkers will be obtained 1, 2, 3, hours post admission and again at 6-12, 24 & 48 hours if still in hospital or attending an outpatient clinic Patients will be followed up for 30 day and 6 month events for the composite end-point of: All cause mortality and/or new ACS and/or readmission to hospital with arrhythmia or heart failure. This research has the potential to speed up diagnosis and ultimately improve outcomes for patients with ACS.

Interventions

We will measure serial B-type Natriuretic Peptide signal peptide (BNP-SP)concentrations in 2000 patients presenting to the Emergency Department within 24 hours of symptom onset of possible Acute Coronary Syndrome (ACS). Clinical history and physical examination will be undertaken. Venous blood samples for cardiac biomarkers will be obtained at 1, 2, 3, hours post admission and again at 6-12, 24 & 48 hours if still in hospital or attend an outpatient clinic. Patients will be followed up for 30

We will measure serial B-type Natriuretic Peptide signal peptide (BNP-SP)concentrations in 2000 patients presenting to the Emergency Department within 24 hours of symptom onset of possible Acute Coronary Syndrome (ACS). Clinical history and physical examination will be undertaken. Venous blood samples for cardiac biomarkers will be obtained at 1, 2, 3, hours post admission and again at 6-12, 24 & 48 hours if still in hospital or attend an outpatient clinic. Patients will be followed up for 30 day and 6 month events for the composite end-point of: All cause mortality and/or new ACS and/or readmission to hospital with arrhythmia or heart failure.

Sponsors

Health Research Council of New Zealand
Lead SponsorGovernment body

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Male or female 18 years of age or older presenting to hospital with possible acute coronary syndrome

Exclusion criteria

Unable to give informed consent Unable to comply with study requirements

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 19, 2026