ID

11723

Descripción

The purpose of this study is to evaluate two approaches to red blood cell transfusion in anemic patients with acute coronary syndrome. https://clinicaltrials.gov/ct2/show/NCT01167582

Link

https://clinicaltrials.gov/ct2/show/NCT01167582

Palabras clave

  1. 28/7/15 28/7/15 -
Subido en

28 de julio de 2015

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility MINT Acute Coronary Syndrome NCT01167582

Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Inclusion Criteria
Descripción

Inclusion Criteria

age 18 or older
Descripción

age 18 or older

Tipo de datos

boolean

Alias
UMLS CUI-1
C0001779
STEMI (ST segment elevated myocardial infarction)
Descripción

STEMI (ST segment elevated myocardial infarction)

Tipo de datos

boolean

Alias
UMLS CUI-1
C1536220
NSTEMI (Non ST segment elevation myocardial infarction)
Descripción

NSTEMI (Non ST segment elevation myocardial infarction)

Tipo de datos

boolean

Alias
UMLS CUI-1
C3537184
unstable angina
Descripción

unstable angina

Tipo de datos

boolean

Alias
UMLS CUI-1
C0002965
stable coronary artery disease
Descripción

stable coronary artery disease

Tipo de datos

boolean

Alias
UMLS CUI-1
C1956346
undergoing cardiac catheterization during the index hospitalization
Descripción

undergoing cardiac catheterization during the index hospitalization

Tipo de datos

boolean

Alias
UMLS CUI-1
C0018795
written informed consent has been obtained
Descripción

written informed consent has been obtained

Tipo de datos

boolean

Alias
UMLS CUI-1
C0021430
hemoglobin concentration less than 10 g/dL at the time of random allocation.
Descripción

hemoglobin concentration less than 10 g/dL at the time of random allocation.

Tipo de datos

boolean

Alias
UMLS CUI-1
C0518015
Exclusion Criteria
Descripción

Exclusion Criteria

bleeding cannot be controlled at the cardiac catheterization puncture site and/or require surgery to repair vessel
Descripción

bleeding cannot be controlled at the cardiac catheterization puncture site and/or require surgery to repair vessel

Tipo de datos

boolean

Alias
UMLS CUI-1
C0019080
retroperitoneal bleeding requiring surgery
Descripción

retroperitoneal bleeding requiring surgery

Tipo de datos

boolean

Alias
UMLS CUI-1
C0019080
clinically important hemodynamic instability based on the judgment of the treating physician
Descripción

clinically important hemodynamic instability based on the judgment of the treating physician

Tipo de datos

boolean

Alias
UMLS CUI-1
C0948268
terminal malignancy or life expectancy less than 6 months
Descripción

terminal malignancy or life expectancy less than 6 months

Tipo de datos

boolean

Alias
UMLS CUI-1
C0679247
scheduled for cardiac surgery within the next 30 days
Descripción

scheduled for cardiac surgery within the next 30 days

Tipo de datos

boolean

Alias
UMLS CUI-1
C0018821
declines blood transfusion
Descripción

declines blood transfusion

Tipo de datos

boolean

Alias
UMLS CUI-1
C3697151
history of a clinically significant transfusion reaction
Descripción

history of a clinically significant transfusion reaction

Tipo de datos

boolean

Alias
UMLS CUI-1
C0274435
inability to provide informed consent;
Descripción

inability to provide informed consent;

Tipo de datos

boolean

Alias
UMLS CUI-1
C0021430
enrolled in a competing study
Descripción

enrolled in a competing study

Tipo de datos

boolean

Alias
UMLS CUI-1
C0422740

Similar models

Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Inclusion Criteria
Age
Item
age 18 or older
boolean
C0001779 (UMLS CUI-1)
STEMI
Item
STEMI (ST segment elevated myocardial infarction)
boolean
C1536220 (UMLS CUI-1)
NSTEMI
Item
NSTEMI (Non ST segment elevation myocardial infarction)
boolean
C3537184 (UMLS CUI-1)
Unstable angina
Item
unstable angina
boolean
C0002965 (UMLS CUI-1)
Coronary artery disease
Item
stable coronary artery disease
boolean
C1956346 (UMLS CUI-1)
Cardiac catheterization
Item
undergoing cardiac catheterization during the index hospitalization
boolean
C0018795 (UMLS CUI-1)
Informed consent
Item
written informed consent has been obtained
boolean
C0021430 (UMLS CUI-1)
Hemoglobin
Item
hemoglobin concentration less than 10 g/dL at the time of random allocation.
boolean
C0518015 (UMLS CUI-1)
Item Group
Exclusion Criteria
Hemorrhage
Item
bleeding cannot be controlled at the cardiac catheterization puncture site and/or require surgery to repair vessel
boolean
C0019080 (UMLS CUI-1)
Hemorrhage
Item
retroperitoneal bleeding requiring surgery
boolean
C0019080 (UMLS CUI-1)
Hemodynamic instability
Item
clinically important hemodynamic instability based on the judgment of the treating physician
boolean
C0948268 (UMLS CUI-1)
Terminal illness
Item
terminal malignancy or life expectancy less than 6 months
boolean
C0679247 (UMLS CUI-1)
Cardiac surgery
Item
scheduled for cardiac surgery within the next 30 days
boolean
C0018821 (UMLS CUI-1)
Blood transfusion declined
Item
declines blood transfusion
boolean
C3697151 (UMLS CUI-1)
Transfusion Reaction
Item
history of a clinically significant transfusion reaction
boolean
C0274435 (UMLS CUI-1)
Informed consent
Item
inability to provide informed consent;
boolean
C0021430 (UMLS CUI-1)
Study patient
Item
enrolled in a competing study
boolean
C0422740 (UMLS CUI-1)

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