ID

33855

Description

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

Link

https://clinicaltrials.gov/show/NCT01495520

Keywords

  1. 1/4/19 1/4/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 4, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Ischemic Heart Disease NCT01495520

Eligibility Ischemic Heart Disease NCT01495520

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
symptoms of palpitations
Description

Symptoms Palpitations

Data type

boolean

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

Coronary Artery Disease Angiography

Data type

boolean

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

Patient's condition stable

Data type

boolean

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

Acute Coronary Syndrome Absent

Data type

boolean

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

Informed Consent

Data type

boolean

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

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

Data type

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
Description

Exclusion Criteria

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

Childbearing Potential Pregnancy test negative

Data type

boolean

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

Kidney Failure Severe

Data type

boolean

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

Liver Failure Severe

Data type

boolean

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

Similar models

Eligibility Ischemic Heart Disease NCT01495520

Name
Type
Description | Question | Decode (Coded Value)
Data type
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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