ID

34306

Beskrivning

Vitamin D Supplementation for Treatment of Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT01230307

Länk

https://clinicaltrials.gov/show/NCT01230307

Nyckelord

  1. 2019-01-16 2019-01-16 -
Rättsinnehavare

GSK group of companies

Uppladdad den

16 januari 2019

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Heart Failure NCT01230307

Eligibility Heart Failure NCT01230307

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
hf patients with lv systolic dysfunction of ischemic or non-ischemic origin and an lvef <40% using nuclear ventriculography or echocardiography within the last 6 months.
Beskrivning

ID.1

Datatyp

boolean

attempts should have been made at optimizing medical therapy and the participant should be stable on these medications for at least 3 months.
Beskrivning

ID.2

Datatyp

boolean

patients with a 25(oh)d level between 10-25 ng/ml
Beskrivning

ID.3

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
inability to give informed consent
Beskrivning

ID.4

Datatyp

boolean

patients with sarcoidosis or other granulomatous disease that can alter vitamin d metabolism
Beskrivning

ID.5

Datatyp

boolean

patients with primary valvular hf, hypertrophic cardiomyopathy, and drug-induced hf
Beskrivning

ID.6

Datatyp

boolean

renal dysfunction defined as serum creatinine > 2.5 mg/dl
Beskrivning

ID.7

Datatyp

boolean

pregnant women
Beskrivning

ID.8

Datatyp

boolean

patients <18 years of age
Beskrivning

ID.9

Datatyp

boolean

patients on vitamin d supplementation
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Heart Failure NCT01230307

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
hf patients with lv systolic dysfunction of ischemic or non-ischemic origin and an lvef <40% using nuclear ventriculography or echocardiography within the last 6 months.
boolean
ID.2
Item
attempts should have been made at optimizing medical therapy and the participant should be stable on these medications for at least 3 months.
boolean
ID.3
Item
patients with a 25(oh)d level between 10-25 ng/ml
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
inability to give informed consent
boolean
ID.5
Item
patients with sarcoidosis or other granulomatous disease that can alter vitamin d metabolism
boolean
ID.6
Item
patients with primary valvular hf, hypertrophic cardiomyopathy, and drug-induced hf
boolean
ID.7
Item
renal dysfunction defined as serum creatinine > 2.5 mg/dl
boolean
ID.8
Item
pregnant women
boolean
ID.9
Item
patients <18 years of age
boolean
ID.10
Item
patients on vitamin d supplementation
boolean

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