ID

33855

Beschreibung

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

Link

https://clinicaltrials.gov/show/NCT01495520

Stichworte

  1. 04.01.19 04.01.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

4. Januar 2019

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Ischemic Heart Disease NCT01495520

Eligibility Ischemic Heart Disease NCT01495520

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
symptoms of palpitations
Beschreibung

Symptoms Palpitations

Datentyp

boolean

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

Coronary Artery Disease Angiography

Datentyp

boolean

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

Patient's condition stable

Datentyp

boolean

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

Acute Coronary Syndrome Absent

Datentyp

boolean

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

Informed Consent

Datentyp

boolean

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

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

Datentyp

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
Beschreibung

Exclusion Criteria

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

Childbearing Potential Pregnancy test negative

Datentyp

boolean

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

Kidney Failure Severe

Datentyp

boolean

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

Liver Failure Severe

Datentyp

boolean

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

Ähnliche Modelle

Eligibility Ischemic Heart Disease NCT01495520

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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