ID

27552

Descripción

The Role of Nitric Oxide Synthase in Circulating Progenitor Cell Function; ODM derived from: https://clinicaltrials.gov/show/NCT00627068

Link

https://clinicaltrials.gov/show/NCT00627068

Palabras clave

Versiones (1)
  1. 20/11/17 20/11/17 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

20 de noviembre de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Cardiovascular Disease NCT00627068

Inglés

Eligibility Cardiovascular Disease NCT00627068

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
willing and able to give written informed consent and comply with study requirements
Descripción

Informed Consent | Protocol Compliance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0525058
adult of 18 years or older
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
subjects willing to provide blood and tissue samples
Descripción

Blood specimen Available | Tissue specimen Available

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0178913
UMLS CUI [1,2]
C0470187
UMLS CUI [2,1]
C1292533
UMLS CUI [2,2]
C0470187
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
failure to give informed consent.
Descripción

Informed Consent failed

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0231175
those unable to consent for themselves.
Descripción

Informed Consent Unable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
those who cannot read english.
Descripción

Lacking Able to read English Language

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0586740
UMLS CUI [1,3]
C0376245
patients on viagra, levitra, or cialis
Descripción

Viagra | Levitra | Cialis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0663448
UMLS CUI [2]
C1174890
UMLS CUI [3]
C0967376
patients with malignant disease
Descripción

Malignant Neoplasms

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
patients with hematological abnormalities
Descripción

Abnormality Hematologic

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1704258
UMLS CUI [1,2]
C0205488
patients with fevers of unknown origin
Descripción

Fever of Unknown Origin

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0015970
severe comorbidity or alcohol/drug dependence
Descripción

Comorbidity Severe | Substance Dependence

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0038580
women who are post-menopausal and on hormone replacement therapy, or premenopausal and on birth control pills (premenopausal women will be screened verbally and then by assay of lh and fsh levels in blood samples to identify women in the follicular phase of their menstrual cycle, to reduce variability)
Descripción

Postmenopausal state | Hormone replacement therapy | Premenopausal status Oral Contraceptives | Premenopausal status Screening Verbal | Premenopausal status Luteinizing hormone measurement Blood specimen | Premenopausal status Follicle stimulating hormone measurement Blood specimen

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232970
UMLS CUI [2]
C0282402
UMLS CUI [3,1]
C0279752
UMLS CUI [3,2]
C0009905
UMLS CUI [4,1]
C0279752
UMLS CUI [4,2]
C0220908
UMLS CUI [4,3]
C0439824
UMLS CUI [5,1]
C0279752
UMLS CUI [5,2]
C0202123
UMLS CUI [5,3]
C0178913
UMLS CUI [6,1]
C0279752
UMLS CUI [6,2]
C0202022
UMLS CUI [6,3]
C0178913
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Similar models

Eligibility Cardiovascular Disease NCT00627068

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent | Protocol Compliance
Item
willing and able to give written informed consent and comply with study requirements
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
Age
Item
adult of 18 years or older
boolean
C0001779 (UMLS CUI [1])
Blood specimen Available | Tissue specimen Available
Item
subjects willing to provide blood and tissue samples
boolean
C0178913 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C1292533 (UMLS CUI [2,1])
C0470187 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Informed Consent failed
Item
failure to give informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
Informed Consent Unable
Item
those unable to consent for themselves.
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Lacking Able to read English Language
Item
those who cannot read english.
boolean
C0332268 (UMLS CUI [1,1])
C0586740 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
Viagra | Levitra | Cialis
Item
patients on viagra, levitra, or cialis
boolean
C0663448 (UMLS CUI [1])
C1174890 (UMLS CUI [2])
C0967376 (UMLS CUI [3])
Malignant Neoplasms
Item
patients with malignant disease
boolean
C0006826 (UMLS CUI [1])
Abnormality Hematologic
Item
patients with hematological abnormalities
boolean
C1704258 (UMLS CUI [1,1])
C0205488 (UMLS CUI [1,2])
Fever of Unknown Origin
Item
patients with fevers of unknown origin
boolean
C0015970 (UMLS CUI [1])
Comorbidity Severe | Substance Dependence
Item
severe comorbidity or alcohol/drug dependence
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0038580 (UMLS CUI [2])
Postmenopausal state | Hormone replacement therapy | Premenopausal status Oral Contraceptives | Premenopausal status Screening Verbal | Premenopausal status Luteinizing hormone measurement Blood specimen | Premenopausal status Follicle stimulating hormone measurement Blood specimen
Item
women who are post-menopausal and on hormone replacement therapy, or premenopausal and on birth control pills (premenopausal women will be screened verbally and then by assay of lh and fsh levels in blood samples to identify women in the follicular phase of their menstrual cycle, to reduce variability)
boolean
C0232970 (UMLS CUI [1])
C0282402 (UMLS CUI [2])
C0279752 (UMLS CUI [3,1])
C0009905 (UMLS CUI [3,2])
C0279752 (UMLS CUI [4,1])
C0220908 (UMLS CUI [4,2])
C0439824 (UMLS CUI [4,3])
C0279752 (UMLS CUI [5,1])
C0202123 (UMLS CUI [5,2])
C0178913 (UMLS CUI [5,3])
C0279752 (UMLS CUI [6,1])
C0202022 (UMLS CUI [6,2])
C0178913 (UMLS CUI [6,3])
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