ID

33855

Descripción

Ranolazine for Improving Symptoms of Palpitations; ODM derived from: https://clinicaltrials.gov/show/NCT01495520

Link

https://clinicaltrials.gov/show/NCT01495520

Palabras clave

  1. 4/1/19 4/1/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

4 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Ischemic Heart Disease NCT01495520

Eligibility Ischemic Heart Disease NCT01495520

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
symptoms of palpitations
Descripción

Symptoms Palpitations

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1457887
UMLS CUI [1,2]
C0030252
angiographically-proven coronary artery disease
Descripción

Coronary Artery Disease Angiography

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1956346
UMLS CUI [1,2]
C0002978
stable conditions
Descripción

Patient's condition stable

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1282982
no recent acute coronary syndromes
Descripción

Acute Coronary Syndrome Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0948089
UMLS CUI [1,2]
C0332197
able to understand and willing to sign the informed consent form
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
symptomatic patients (palpitation) with stable angina pectoris already on therapy with beta-blockers and/or calcium antagonists.
Descripción

Palpitations Symptomatic | Stable angina | Adrenergic beta-1 Receptor Antagonists | Calcium Channel Blockers

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030252
UMLS CUI [1,2]
C0231220
UMLS CUI [2]
C0340288
UMLS CUI [3]
C0304516
UMLS CUI [4]
C0006684
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
women of child bearing potential patients must demonstrate a negative pregnancy test performed within 24 hours
Descripción

Childbearing Potential Pregnancy test negative

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0427780
severe renal failure
Descripción

Kidney Failure Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0035078
UMLS CUI [1,2]
C0205082
severe hepatic failure
Descripción

Liver Failure Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0085605
UMLS CUI [1,2]
C0205082

Similar models

Eligibility Ischemic Heart Disease NCT01495520

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Symptoms Palpitations
Item
symptoms of palpitations
boolean
C1457887 (UMLS CUI [1,1])
C0030252 (UMLS CUI [1,2])
Coronary Artery Disease Angiography
Item
angiographically-proven coronary artery disease
boolean
C1956346 (UMLS CUI [1,1])
C0002978 (UMLS CUI [1,2])
Patient's condition stable
Item
stable conditions
boolean
C1282982 (UMLS CUI [1])
Acute Coronary Syndrome Absent
Item
no recent acute coronary syndromes
boolean
C0948089 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Informed Consent
Item
able to understand and willing to sign the informed consent form
boolean
C0021430 (UMLS CUI [1])
Palpitations Symptomatic | Stable angina | Adrenergic beta-1 Receptor Antagonists | Calcium Channel Blockers
Item
symptomatic patients (palpitation) with stable angina pectoris already on therapy with beta-blockers and/or calcium antagonists.
boolean
C0030252 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0340288 (UMLS CUI [2])
C0304516 (UMLS CUI [3])
C0006684 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Childbearing Potential Pregnancy test negative
Item
women of child bearing potential patients must demonstrate a negative pregnancy test performed within 24 hours
boolean
C3831118 (UMLS CUI [1,1])
C0427780 (UMLS CUI [1,2])
Kidney Failure Severe
Item
severe renal failure
boolean
C0035078 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Liver Failure Severe
Item
severe hepatic failure
boolean
C0085605 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])

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