Phase
Condition
Coronary Artery Disease
Myocardial Ischemia
Hypercholesterolemia
Treatment
Implementation of the new population and sex-specific 99th percentile URL for cardiac troponin
Clinical Study ID
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion criteria for the primary cohort:
The primary cohort will include the women and men who are expected to be most significantly impacted by the intervention, and this group is specifically defined by
Presenting complaints suggestive of ACS
At least one cTn measurement within 24 hours of admission
A peak cTn value between the current sex-uniform manufacturer-derived 99thpercentile URL and the novel sex-and population-specific 99th percentile URLs forwomen and men.
Presenting complaints suggestive of ACS will be identified in hospital records by the following presenting complaints of "chest pain" (DR074), "angina pectoris" (DI20), "observation due to suspicion of myocardial infarction" (Z034), "myocardial infarction" (DI21), "abdominal and pelvic pain" (DR10), "pain in the throat and chest" (DR07), "dyspnea" (DR060), "reflux" (DK21), "ischemic heart disease" (DI22-DI25) and "observation due to suspicion of another cardiovascular disorder" (DZ035).
Study participants are included at their index admission, and subsequent admissions are evaluated in follow up analyses.
Exclusion
Exclusion criteria:
Age < 18 years
Patients with discharge diagnoses with conditions like pericarditis, myocarditis,endocarditis, cardiomyopathy, valve disease, arrhythmia, heart failure, pulmonaryembolism, respiratory diseases, infectious diseases, digestive system diseasesexcluding reflux, digestive system diseases, diseases of the urinary andreproductive organs, and diseases of bones, muscles, and connective tissue, and donot have a discharge diagnosis of myocardial infarction or angina pectoris
The initial month following the implementation of the new sex-specific 99th percentile URLs will be excluded from consideration, as it will be seen as an adjustment period. Consequently, the intervention period will be extended by one month.
Study Design
Study Description
Connect with a study center
Hospital of Southern Jutland
Aabenraa, 6200
DenmarkSite Not Available
Aalborg University Hospital
Aalborg, 9000
DenmarkSite Not Available
Aarhus University Hospital
Aarhus, 8000
DenmarkSite Not Available
Bispebjerg & Frederiksberg Hospital
Bispebjerg, 2400
DenmarkSite Not Available
Rigshospitalet (Blegdamsvej)
Copenhagen Ø, 2100
DenmarkSite Not Available
Sydvestjysk Sygehus
Esbjerg, 6700
DenmarkSite Not Available
Glostrup University Hospital
Glostrup, 2600
DenmarkSite Not Available
Glostrup University Hospital
Glostrup Municipality, 2600
DenmarkSite Not Available
Gødstrup Regional Hospital
Gødstrup, 7400
DenmarkSite Not Available
Herlev & Gentofte Hospital
Herlev, 2730
DenmarkSite Not Available
C Torp-Pedersen
Hillerød, 3400
DenmarkSite Not Available
North Denmark Regional Hospital
Hjørring, 9800
DenmarkSite Not Available
Holbaek Sygehus
Holbæk, 4300
DenmarkSite Not Available
Horsens Hospital
Horsens, 8700
DenmarkSite Not Available
Amager & Hvidovre Hospital
Hvidovre, 2650
DenmarkSite Not Available
Sygehus Lillebælt (Kolding Sygehus & Vejle Sygehus)
Kolding, 6000
DenmarkSite Not Available
Zealand University Hospital
Køge, 4600
DenmarkSite Not Available
Nykøbing Falster County Hospital
Nykøbing Falster, 4800
DenmarkSite Not Available
Odense University Hospital
Odense, 5000
DenmarkSite Not Available
Randers Regional Hospital
Randers, 8930
DenmarkSite Not Available
Slagelse Sygehus
Slagelse, 4200
DenmarkSite Not Available
Svendborg Hospital
Svendborg, 5700
DenmarkSite Not Available
Central Jutland Regional Hospital (Viborg Hospital & Silkeborg Hospital)
Viborg, 8800
DenmarkSite Not Available

Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.