ID

34306

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT01230307

Trefwoorden

  1. 16-01-19 16-01-19 -
Houder van rechten

GSK group of companies

Geüploaded op

16 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Heart Failure NCT01230307

Eligibility Heart Failure NCT01230307

Inclusion Criteria
Beschrijving

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.
Beschrijving

ID.1

Datatype

boolean

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

ID.2

Datatype

boolean

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

ID.3

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
inability to give informed consent
Beschrijving

ID.4

Datatype

boolean

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

ID.5

Datatype

boolean

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

ID.6

Datatype

boolean

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

ID.7

Datatype

boolean

pregnant women
Beschrijving

ID.8

Datatype

boolean

patients <18 years of age
Beschrijving

ID.9

Datatype

boolean

patients on vitamin d supplementation
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Heart Failure NCT01230307

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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