ID

12770

Beskrivning

Effect of Ischemic Postconditioning on Targeting of Annexin A5 After Forearm Exercise; ODM derived from: https://clinicaltrials.gov/show/NCT00441714

Länk

https://clinicaltrials.gov/show/NCT00441714

Nyckelord

  1. 2015-12-21 2015-12-21 -
Uppladdad den

21 december 2015

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Cardiovascular Disease NCT00441714

Eligibility Cardiovascular Disease NCT00441714

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 18-50 years
Beskrivning

age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
no physical limitation to perform ischemic exercise
Beskrivning

exercise ischemic

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0015259
UMLS CUI [1,2]
C0475224
informed consent
Beskrivning

informed consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
diabetes (fasting glucose > 7,0mmol/l, or random glucose >11,0mmol/l)
Beskrivning

diabetes; fasting glucose measurement; Glucose measurement, random

Datatyp

boolean

Alias
UMLS CUI [1]
C0011849
UMLS CUI [2]
C0202045
UMLS CUI [3]
C0202046
hyperlipidemia (random total cholesterol > 6.5 mmol/l)
Beskrivning

hyperlipidemia

Datatyp

boolean

Alias
UMLS CUI [1]
C0020473
hypertension (supine sbp/dbp > 140/90 mmhg at screening)
Beskrivning

hypertension

Datatyp

boolean

Alias
UMLS CUI [1]
C0020538
any cardiovascular disease
Beskrivning

cardiovascular disease

Datatyp

boolean

Alias
UMLS CUI [1]
C0007222
drug abuse
Beskrivning

drug abuse

Datatyp

boolean

Alias
UMLS CUI [1]
C0013146
concomitant chronic use of medication
Beskrivning

concomitant medication

Datatyp

boolean

Alias
UMLS CUI [1]
C2347852
administration of radioactivity in research setting during the last 5 years
Beskrivning

radiotherapy

Datatyp

boolean

Alias
UMLS CUI [1]
C1522449
participation to any drug-investigation during the previous month as checked with vip check according to crcn standard procedures.
Beskrivning

Study Subject Participation Status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Cardiovascular Disease NCT00441714

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
age 18-50 years
boolean
C0001779 (UMLS CUI [1])
exercise ischemic
Item
no physical limitation to perform ischemic exercise
boolean
C0015259 (UMLS CUI [1,1])
C0475224 (UMLS CUI [1,2])
informed consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
diabetes; fasting glucose measurement; Glucose measurement, random
Item
diabetes (fasting glucose > 7,0mmol/l, or random glucose >11,0mmol/l)
boolean
C0011849 (UMLS CUI [1])
C0202045 (UMLS CUI [2])
C0202046 (UMLS CUI [3])
hyperlipidemia
Item
hyperlipidemia (random total cholesterol > 6.5 mmol/l)
boolean
C0020473 (UMLS CUI [1])
hypertension
Item
hypertension (supine sbp/dbp > 140/90 mmhg at screening)
boolean
C0020538 (UMLS CUI [1])
cardiovascular disease
Item
any cardiovascular disease
boolean
C0007222 (UMLS CUI [1])
drug abuse
Item
drug abuse
boolean
C0013146 (UMLS CUI [1])
concomitant medication
Item
concomitant chronic use of medication
boolean
C2347852 (UMLS CUI [1])
radiotherapy
Item
administration of radioactivity in research setting during the last 5 years
boolean
C1522449 (UMLS CUI [1])
Study Subject Participation Status
Item
participation to any drug-investigation during the previous month as checked with vip check according to crcn standard procedures.
boolean
C2348568 (UMLS CUI [1])

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