CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Biomarker (TropT, Myoglobin, CK, CK-MB, LDH, D-dimer, CRP, PCT)Wiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (0)


Name (Synonyms) Correlation

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D016638 Critical Illness NIH 0.14

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 Prospective Observational ICU Trial in Critical Ill COVID‐19 Patients (POINT-C) Cardiovascular Risk and the Effects on Myocardial Events in Critical Ill COVID-19 Patients

The aim of our study is to observe the intensive care course in 30-50 COVID-19 patients with regard to cardiovascular risk factors and biomarkers. The primary objective of this study is to investigate the cardiovascular risk and its impact on cardiovascular complications in COVID-19 patients in intensive care units. This study is designed to investigate correlations and to investigate factors influencing the course of the new viral disease COVID-19 in intensive care. Previous scientific findings are still rare due to the relevance of the disease, therefore this study is also explorative and not exclusively based on a hypothesis. The cardiovascular risk will be assessed upon admission to the intensive care unit and subsequently the course of biomarkers (see below) will be analysed in a cohort study (no, low and high cardiovascular risk).

NCT04349982 Risk Factor, Cardiovascular Covid19 Critical Illness Course Illness Diagnostic Test: Biomarker (TropT, Myoglobin, CK, CK-MB, LDH, D-dimer, CRP, PCT)
MeSH:Critical Illness

Primary Outcomes

Description: Troponin courses in the intensive care unit are analyzed in consideration of the respective cardiovascular risk.

Measure: ICU CV risk and Biomarker (e.g. Troponin)

Time: through study completion, up to 4 weeks

Secondary Outcomes

Description: The 30-day mortality during the ICU stay is determined and divided into appropriate cardiovascular risk groups.

Measure: CV risk and Outcome during ICU stay

Time: through study completion, up to 4 weeks


No related HPO nodes (Using clinical trials)