ID

23442

Descripción

Responsible Party: Martin Moeckel, Head Emergency Medicine, Charite University, Berlin, Germany ClinicalTrials.gov Identifier: NCT01498731 History of Changes Other Study ID Numbers: Charite-BiC-8 DRKS00000276 ( Other Identifier: German Clinical Trials Register ) U1111-1118-1665 ( Registry Identifier: International Clinical Trials Registry Platform ) Study First Received: October 25, 2011 Last Updated: June 4, 2013 Effect of the Biomarker Copeptin in Managing Patients With Suspected Acute Coronary Syndrome (ACS) (BiC-8) ODM derived from: https://clinicaltrials.gov/ct2/show/NCT01498731

Link

https://clinicaltrials.gov/ct2/show/NCT01498731

Palabras clave

  1. 4/7/17 4/7/17 -
Subido en

4 de julio de 2017

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Acute Coronary Syndrome DRKS00000276 NCT01498731 DRKS00000276

Eligibility Acute Coronary Syndrome NCT01498731 DRKS00000276

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
Typical chest pain (with or without ECG-changes, but no ST-elevation)suggestive of unstable angina or non-ST-elevated myocardial infarction (NSTEMI)
Descripción

Chest Pain

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0008031
Troponin negative at admission according to the current clinical practice Patient willing and able to give written informed consent
Descripción

Troponin

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0523952
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Healthy Volunteers
Descripción

Control Group

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009932
Patients with ST-elevation myocardial infarction (STEMI)
Descripción

ST-elevation myocardial infarction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1536220
Continuing chest pain or recurrent episodes of chest pain under therapy
Descripción

Chest Pain Specification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0008031
UMLS CUI [1,2]
C2348235
High-risk patients with suspected ACS who need to be hospitalized for reasons independent of their initial troponin result
Descripción

Hospitalization

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019993
Patients who need to be hospitalized for other medical reasons
Descripción

Hospitalization for other medical reasons

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C3841427
Patients in need of urgent life-saving interventions
Descripción

Requires immediate life-saving intervention

Tipo de datos

boolean

Alias
UMLS CUI [1]
C4264611
Patients under 18 years of age
Descripción

Age

Tipo de datos

boolean

Patients with a life expectancy < 6 months
Descripción

Life Expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
Patients with any condition that leads the treating physician to not consider the patient eligible for the trial
Descripción

Eligibility Determination

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013893

Similar models

Eligibility Acute Coronary Syndrome NCT01498731 DRKS00000276

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
Chest Pain
Item
Typical chest pain (with or without ECG-changes, but no ST-elevation)suggestive of unstable angina or non-ST-elevated myocardial infarction (NSTEMI)
boolean
C0008031 (UMLS CUI [1])
Troponin
Item
Troponin negative at admission according to the current clinical practice Patient willing and able to give written informed consent
boolean
C0523952 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
Control Group
Item
Healthy Volunteers
boolean
C0009932 (UMLS CUI [1])
ST-elevation myocardial infarction
Item
Patients with ST-elevation myocardial infarction (STEMI)
boolean
C1536220 (UMLS CUI [1])
Chest Pain Specification
Item
Continuing chest pain or recurrent episodes of chest pain under therapy
boolean
C0008031 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Hospitalization
Item
High-risk patients with suspected ACS who need to be hospitalized for reasons independent of their initial troponin result
boolean
C0019993 (UMLS CUI [1])
Hospitalization for other medical reasons
Item
Patients who need to be hospitalized for other medical reasons
boolean
C0019993 (UMLS CUI [1,1])
C3841427 (UMLS CUI [1,2])
Requires immediate life-saving intervention
Item
Patients in need of urgent life-saving interventions
boolean
C4264611 (UMLS CUI [1])
Age
Item
Patients under 18 years of age
boolean
Life Expectancy
Item
Patients with a life expectancy < 6 months
boolean
C0023671 (UMLS CUI [1])
Eligibility Determination
Item
Patients with any condition that leads the treating physician to not consider the patient eligible for the trial
boolean
C0013893 (UMLS CUI [1])

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial