ID

39912

Beskrivning

The Effect of Hypertension Medications on Renal Blood Flow Measurements in Healthy Males; ODM derived from: https://clinicaltrials.gov/show/NCT00856960

Länk

https://clinicaltrials.gov/show/NCT00856960

Nyckelord

Versioner (1)
  1. 2020-03-03 2020-03-03 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

3 mars 2020

DOI

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Licens

Creative Commons BY 4.0
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Eligibility Hypertension NCT00856960

Engelsk

Eligibility Hypertension NCT00856960

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject is in generally good health
Beskrivning

General health good

Datatyp

boolean

Alias
UMLS CUI [1]
C1277245
subject is willing to avoid unaccustomed strenuous exercise during the study
Beskrivning

Avoidance Strenuous Exercise

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0870186
UMLS CUI [1,2]
C1514989
subject agrees to consume only the study-specified diet during all domiciled periods
Beskrivning

Diet therapy Study Protocol Specified

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0012159
UMLS CUI [1,2]
C2348563
UMLS CUI [1,3]
C0205369
subject has been a non-smoker for at least 3 months prior to study
Beskrivning

Non-smoker

Datatyp

boolean

Alias
UMLS CUI [1]
C0337672
subject will refrain from smoking or using any tobacco products during the study
Beskrivning

Refrain from Smoking | Tobacco use Absent

Datatyp

boolean

Alias
UMLS CUI [1]
C4086797
UMLS CUI [2,1]
C0543414
UMLS CUI [2,2]
C0332197
subject agrees to refrain from consuming alcohol or caffeine during the domiciled periods and agrees to limit alcohol and caffeine consumption throughout the study
Beskrivning

Avoidance Alcohol consumption | Avoidance Caffeine ingestion

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0870186
UMLS CUI [1,2]
C0001948
UMLS CUI [2,1]
C0870186
UMLS CUI [2,2]
C0238877
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
subject has contraindication to mri scans
Beskrivning

Medical contraindication MRI scan

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
subject has a history of stroke, seizure, or major neurological disorders
Beskrivning

Cerebrovascular accident | Seizure | Nervous system disorder Major

Datatyp

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0036572
UMLS CUI [3,1]
C0027765
UMLS CUI [3,2]
C0205164
subject uses illicit drugs or has a history of drug/alcohol abuse
Beskrivning

Illicit medication use | Substance Use Disorders

Datatyp

boolean

Alias
UMLS CUI [1]
C0281875
UMLS CUI [2]
C0038586
subject has had major surgery, has donated or lost 1 unit of blood, or has been in another investigational study in the last 4 weeks
Beskrivning

Major surgery | Blood Donation Unit Quantity | Blood Loss Unit Quantity | Study Subject Participation Status | Research study

Datatyp

boolean

Alias
UMLS CUI [1]
C0679637
UMLS CUI [2,1]
C0005794
UMLS CUI [2,2]
C0439148
UMLS CUI [2,3]
C1265611
UMLS CUI [3,1]
C3163616
UMLS CUI [3,2]
C0439148
UMLS CUI [3,3]
C1265611
UMLS CUI [4]
C2348568
UMLS CUI [5]
C0681814
subject has a history of multiple and/or severe allergies to drugs or food
Beskrivning

Drug Allergy Multiple | Food Allergy Multiple | Drug Allergy Severe | Food Allergy Severe

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0013182
UMLS CUI [1,2]
C0439064
UMLS CUI [2,1]
C0016470
UMLS CUI [2,2]
C0439064
UMLS CUI [3,1]
C0013182
UMLS CUI [3,2]
C0205082
UMLS CUI [4,1]
C0016470
UMLS CUI [4,2]
C0205082
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Similar models

Eligibility Hypertension NCT00856960

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
General health good
Item
subject is in generally good health
boolean
C1277245 (UMLS CUI [1])
Avoidance Strenuous Exercise
Item
subject is willing to avoid unaccustomed strenuous exercise during the study
boolean
C0870186 (UMLS CUI [1,1])
C1514989 (UMLS CUI [1,2])
Diet therapy Study Protocol Specified
Item
subject agrees to consume only the study-specified diet during all domiciled periods
boolean
C0012159 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Non-smoker
Item
subject has been a non-smoker for at least 3 months prior to study
boolean
C0337672 (UMLS CUI [1])
Refrain from Smoking | Tobacco use Absent
Item
subject will refrain from smoking or using any tobacco products during the study
boolean
C4086797 (UMLS CUI [1])
C0543414 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Avoidance Alcohol consumption | Avoidance Caffeine ingestion
Item
subject agrees to refrain from consuming alcohol or caffeine during the domiciled periods and agrees to limit alcohol and caffeine consumption throughout the study
boolean
C0870186 (UMLS CUI [1,1])
C0001948 (UMLS CUI [1,2])
C0870186 (UMLS CUI [2,1])
C0238877 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Medical contraindication MRI scan
Item
subject has contraindication to mri scans
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
Cerebrovascular accident | Seizure | Nervous system disorder Major
Item
subject has a history of stroke, seizure, or major neurological disorders
boolean
C0038454 (UMLS CUI [1])
C0036572 (UMLS CUI [2])
C0027765 (UMLS CUI [3,1])
C0205164 (UMLS CUI [3,2])
Illicit medication use | Substance Use Disorders
Item
subject uses illicit drugs or has a history of drug/alcohol abuse
boolean
C0281875 (UMLS CUI [1])
C0038586 (UMLS CUI [2])
Major surgery | Blood Donation Unit Quantity | Blood Loss Unit Quantity | Study Subject Participation Status | Research study
Item
subject has had major surgery, has donated or lost 1 unit of blood, or has been in another investigational study in the last 4 weeks
boolean
C0679637 (UMLS CUI [1])
C0005794 (UMLS CUI [2,1])
C0439148 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C3163616 (UMLS CUI [3,1])
C0439148 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
C2348568 (UMLS CUI [4])
C0681814 (UMLS CUI [5])
Drug Allergy Multiple | Food Allergy Multiple | Drug Allergy Severe | Food Allergy Severe
Item
subject has a history of multiple and/or severe allergies to drugs or food
boolean
C0013182 (UMLS CUI [1,1])
C0439064 (UMLS CUI [1,2])
C0016470 (UMLS CUI [2,1])
C0439064 (UMLS CUI [2,2])
C0013182 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0016470 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
Tillbaka till toppen 

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