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Prospective Registry for Patients With Chest Pain in Emergency Department

Prospective Registry for Patients With Chest Pain in Emergency Department

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05058300
Acronym
ThReg
Enrollment
3000
Registered
2021-09-27
Start date
2017-09-20
Completion date
2024-10-11
Last updated
2023-11-07

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

Conditions

Chest Pain

Keywords

Chest Pain

Brief summary

monocentric, prospective registry collection of clinical data of all patients with chest pain in emergency department and follow-up after 30 days

Detailed description

An unselected patient-population with chest pain entering through the emergency department participate in a diagnostic survey where a chest pain algorithm based mainly on risk scores (Grace, TIMI, Heart) verifying the diagnostic forecasting power (sensitivity, specificity, negative and positive predictive value) of biomarkers, risk scores and imaging methods for diagnosing of potential life-threatening disease.

Interventions

DEVICECT Thorax

CT Thorax (GE Revolution with chest pain algorithm)

Sponsors

Zentrum für Klinische Studien Jena
CollaboratorOTHER
GE Healthcare
CollaboratorINDUSTRY
Jena University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* age \>18 years old chest pain written confirmation of participants or legal representative

Exclusion criteria

* thorax trauma

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic forecast of biomarkers, risk scores and computer tomographyFrom admission to emergency unit dischargeDiagnostic forecast compared to the initial suspected diagnosis and discharge diagnosis

Secondary

MeasureTime frameDescription
SensitivityDuring diagnostic procedureSensitivity in result of biomarkers, risk scores and imaging methods
SpecificityDuring diagnostic procedureSpecificity in result of biomarkers, risk scores and imaging methods
Positive predictive valueDuring diagnostic procedurePositive predictive value in result of biomarkers, risk scores and imaging methods
Negative predictive valueDuring diagnostic procedureNegative predictive value in result of biomarkers, risk scores and imaging methods
Major adverse cardiac events (MACE)From admission to emergency unit until 30 days after or deathoutcome is measured by coronary intervention, coronary bypass and death within 30 days

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026