ID

39479

Beschrijving

Benefit of the Treatment With Testosterone in Chronic Heart Failure Testosterone Deficiency Subjects; ODM derived from: https://clinicaltrials.gov/show/NCT01813201

Link

https://clinicaltrials.gov/show/NCT01813201

Trefwoorden

Versies (1)
  1. 15-01-20 15-01-20 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

15 januari 2020

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Heart Failure NCT01813201

Engels

Eligibility Heart Failure NCT01813201

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
at least one hospital admission for hf.
Beschrijving

Hospitalization Due to Heart Failure Quantity

Datatype

boolean

Alias
UMLS CUI [1,1]
C3898876
UMLS CUI [1,2]
C1265611
stable clinical status, new york heart association (nyha) functional class ii-iv.
Beschrijving

Stable status Clinical | New York Heart Association Classification

Datatype

boolean

Alias
UMLS CUI [1,1]
C0205360
UMLS CUI [1,2]
C0205210
UMLS CUI [2]
C1275491
left ventricular ejection fraction of less than 40%
Beschrijving

Left ventricular ejection fraction

Datatype

boolean

Alias
UMLS CUI [1]
C0428772
nt-probnp concentration greater than 1000 pg / ml.
Beschrijving

N-Terminal ProB-type Natriuretic Peptide Measurement

Datatype

boolean

Alias
UMLS CUI [1]
C3272900
total testosterone and free testosterone deficiency measured in the last month
Beschrijving

Deficiency Total Testosterone Measurement | Deficiency Free Testosterone Measurement

Datatype

boolean

Alias
UMLS CUI [1,1]
C1963961
UMLS CUI [1,2]
C0202227
UMLS CUI [2,1]
C1963961
UMLS CUI [2,2]
C0202228
age >18 years.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
patients who have given their written informed consent.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
no informed consent.
Beschrijving

Informed Consent Lacking

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332268
taking oral anticoagulants
Beschrijving

Oral anticoagulants

Datatype

boolean

Alias
UMLS CUI [1]
C0354604
severe valvular heart disease with an indication for surgical repair.
Beschrijving

Heart valve disease Severe | Indication Surgical repair

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018824
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C0374711
extracardiac disease with an estimated prognosis of less than 1 year.
Beschrijving

Disease Prognosis Estimated | Exception Heart Disease

Datatype

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0033325
UMLS CUI [1,3]
C0750572
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0018799
history of androgen-dependent prostate cancer, benign prostate hyperplasia treatment or prostate-specific antigen (psa)> 3 ng / ml.
Beschrijving

Prostate carcinoma Androgen dependent | Treatment Benign Prostatic Hyperplasia | Prostate specific antigen measurement

Datatype

boolean

Alias
UMLS CUI [1,1]
C0600139
UMLS CUI [1,2]
C0002844
UMLS CUI [1,3]
C1701901
UMLS CUI [2,1]
C0087111
UMLS CUI [2,2]
C1704272
UMLS CUI [3]
C0201544
history of breast carcinoma or liver tumor
Beschrijving

Breast Carcinoma | Liver carcinoma

Datatype

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2]
C2239176
severe renal impairment (glomerular filtration rate <30 ml / kg / min).
Beschrijving

Renal Insufficiency Severe | Glomerular Filtration Rate

Datatype

boolean

Alias
UMLS CUI [1,1]
C1565489
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0017654
acute coronary syndrome in the last year
Beschrijving

Acute Coronary Syndrome

Datatype

boolean

Alias
UMLS CUI [1]
C0948089
renal or hepatic failure
Beschrijving

Kidney Failure | Liver Failure

Datatype

boolean

Alias
UMLS CUI [1]
C0035078
UMLS CUI [2]
C0085605
uncontrolled hypertension
Beschrijving

Uncontrolled hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C1868885
erythrocytosis (hematocrit> 5%)
Beschrijving

Erythrocytosis | Hematocrit procedure

Datatype

boolean

Alias
UMLS CUI [1]
C1527405
UMLS CUI [2]
C0018935
hypersensitivity to testosterone or any excipients.
Beschrijving

Testosterone allergy | Hypersensitivity Testosterone Excipient

Datatype

boolean

Alias
UMLS CUI [1]
C0571682
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0039601
UMLS CUI [2,3]
C0015237
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Similar models

Eligibility Heart Failure NCT01813201

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Hospitalization Due to Heart Failure Quantity
Item
at least one hospital admission for hf.
boolean
C3898876 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Stable status Clinical | New York Heart Association Classification
Item
stable clinical status, new york heart association (nyha) functional class ii-iv.
boolean
C0205360 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C1275491 (UMLS CUI [2])
Left ventricular ejection fraction
Item
left ventricular ejection fraction of less than 40%
boolean
C0428772 (UMLS CUI [1])
N-Terminal ProB-type Natriuretic Peptide Measurement
Item
nt-probnp concentration greater than 1000 pg / ml.
boolean
C3272900 (UMLS CUI [1])
Deficiency Total Testosterone Measurement | Deficiency Free Testosterone Measurement
Item
total testosterone and free testosterone deficiency measured in the last month
boolean
C1963961 (UMLS CUI [1,1])
C0202227 (UMLS CUI [1,2])
C1963961 (UMLS CUI [2,1])
C0202228 (UMLS CUI [2,2])
Age
Item
age >18 years.
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
patients who have given their written informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Informed Consent Lacking
Item
no informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Oral anticoagulants
Item
taking oral anticoagulants
boolean
C0354604 (UMLS CUI [1])
Heart valve disease Severe | Indication Surgical repair
Item
severe valvular heart disease with an indication for surgical repair.
boolean
C0018824 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C0374711 (UMLS CUI [2,2])
Disease Prognosis Estimated | Exception Heart Disease
Item
extracardiac disease with an estimated prognosis of less than 1 year.
boolean
C0012634 (UMLS CUI [1,1])
C0033325 (UMLS CUI [1,2])
C0750572 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C0018799 (UMLS CUI [2,2])
Prostate carcinoma Androgen dependent | Treatment Benign Prostatic Hyperplasia | Prostate specific antigen measurement
Item
history of androgen-dependent prostate cancer, benign prostate hyperplasia treatment or prostate-specific antigen (psa)> 3 ng / ml.
boolean
C0600139 (UMLS CUI [1,1])
C0002844 (UMLS CUI [1,2])
C1701901 (UMLS CUI [1,3])
C0087111 (UMLS CUI [2,1])
C1704272 (UMLS CUI [2,2])
C0201544 (UMLS CUI [3])
Breast Carcinoma | Liver carcinoma
Item
history of breast carcinoma or liver tumor
boolean
C0678222 (UMLS CUI [1])
C2239176 (UMLS CUI [2])
Renal Insufficiency Severe | Glomerular Filtration Rate
Item
severe renal impairment (glomerular filtration rate <30 ml / kg / min).
boolean
C1565489 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0017654 (UMLS CUI [2])
Acute Coronary Syndrome
Item
acute coronary syndrome in the last year
boolean
C0948089 (UMLS CUI [1])
Kidney Failure | Liver Failure
Item
renal or hepatic failure
boolean
C0035078 (UMLS CUI [1])
C0085605 (UMLS CUI [2])
Uncontrolled hypertension
Item
uncontrolled hypertension
boolean
C1868885 (UMLS CUI [1])
Erythrocytosis | Hematocrit procedure
Item
erythrocytosis (hematocrit> 5%)
boolean
C1527405 (UMLS CUI [1])
C0018935 (UMLS CUI [2])
Testosterone allergy | Hypersensitivity Testosterone Excipient
Item
hypersensitivity to testosterone or any excipients.
boolean
C0571682 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C0039601 (UMLS CUI [2,2])
C0015237 (UMLS CUI [2,3])
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