ID

13111

Description

Magnetic Resonance Imaging for Evaluating Kidney Function; ODM derived from: https://clinicaltrials.gov/show/NCT00006173

Link

https://clinicaltrials.gov/show/NCT00006173

Keywords

  1. 1/17/16 1/17/16 -
Uploaded on

January 17, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Healthy NCT00006173

Eligibility Healthy NCT00006173

  1. StudyEvent: Eligibility
    1. Eligibility Healthy NCT00006173
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
healthy volunteers or patients with significant clinical suspicion of renovascular hypertension.
Description

renovascular hypertension

Data type

boolean

Alias
UMLS CUI [1]
C0020545
subjects able to understand the informed consent for this study.
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
subjects must be able to hold their breath for 20 second intervals.
Description

breath holding

Data type

boolean

Alias
UMLS CUI [1]
C0235744
patients must be clinically stable and be judged by their physician able to tolerate the mr study of 1.5-2 hour duration.
Description

health status

Data type

boolean

Alias
UMLS CUI [1]
C0018759
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
any contraindication for mr study including: pacemaker or other implanted electronic device; cochlear implants; metal in the eye; embedded shrapnel fragments; cerebral aneurysm clips; or medical infusion pumps.
Description

mri contraindication

Data type

boolean

Alias
UMLS CUI [1,1]
C0024485
UMLS CUI [1,2]
C1301624
allergy to gadolinium, iodinated contrast media, aceis, or sulphur-containing medication.
Description

hypersensitivity

Data type

boolean

Alias
UMLS CUI [1]
C0020517
patients have a hematocrit at or below 30. severe anemia may predispose to hypotension after captopril.
Description

hematocrit

Data type

boolean

Alias
UMLS CUI [1]
C0518014
patients with hyperkalemia (plasma potassium: above 5.0 mmol/l), because of the risk of arrhythmia.
Description

hyperkalemia

Data type

boolean

Alias
UMLS CUI [1]
C0020461
clinically unstable patients and those unable to tolerate a 1-2 hour mr study. examples of medical conditions that would lead to exclusion include unstable angina, dyspnea at rest, severe pain at rest, or severe back pain.
Description

comorbidity

Data type

boolean

Alias
UMLS CUI [1]
C0009488
pregnancy.
Description

pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
nursing mothers.
Description

lactation

Data type

boolean

Alias
UMLS CUI [1]
C0006147
subjects who are claustrophobic and are unable to tolerate mr imaging.
Description

claustrophobia

Data type

boolean

Alias
UMLS CUI [1]
C0008909
patients with a serum creatinine concentration above 4mg/dl.
Description

creatinine

Data type

boolean

Alias
UMLS CUI [1]
C0201976
bilateral renal stents.
Description

bilateral renal stents

Data type

boolean

Alias
UMLS CUI [1,1]
C1322812
UMLS CUI [1,2]
C0238767
healthy subjects must not have an abnormality detected on dipstick urinalysis, or a systolic bp above 140 mmhg or a diastolic bp above 90 mmhg on screening examination or an abnormal bun or creatinine level in the blood.
Description

dipstick urine test, bp, bun, creatinine

Data type

boolean

Alias
UMLS CUI [1]
C0430370
UMLS CUI [2]
C0005823
UMLS CUI [3]
C0005845
UMLS CUI [4]
C0201976

Similar models

Eligibility Healthy NCT00006173

  1. StudyEvent: Eligibility
    1. Eligibility Healthy NCT00006173
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
renovascular hypertension
Item
healthy volunteers or patients with significant clinical suspicion of renovascular hypertension.
boolean
C0020545 (UMLS CUI [1])
informed consent
Item
subjects able to understand the informed consent for this study.
boolean
C0021430 (UMLS CUI [1])
breath holding
Item
subjects must be able to hold their breath for 20 second intervals.
boolean
C0235744 (UMLS CUI [1])
health status
Item
patients must be clinically stable and be judged by their physician able to tolerate the mr study of 1.5-2 hour duration.
boolean
C0018759 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
mri contraindication
Item
any contraindication for mr study including: pacemaker or other implanted electronic device; cochlear implants; metal in the eye; embedded shrapnel fragments; cerebral aneurysm clips; or medical infusion pumps.
boolean
C0024485 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
hypersensitivity
Item
allergy to gadolinium, iodinated contrast media, aceis, or sulphur-containing medication.
boolean
C0020517 (UMLS CUI [1])
hematocrit
Item
patients have a hematocrit at or below 30. severe anemia may predispose to hypotension after captopril.
boolean
C0518014 (UMLS CUI [1])
hyperkalemia
Item
patients with hyperkalemia (plasma potassium: above 5.0 mmol/l), because of the risk of arrhythmia.
boolean
C0020461 (UMLS CUI [1])
comorbidity
Item
clinically unstable patients and those unable to tolerate a 1-2 hour mr study. examples of medical conditions that would lead to exclusion include unstable angina, dyspnea at rest, severe pain at rest, or severe back pain.
boolean
C0009488 (UMLS CUI [1])
pregnancy
Item
pregnancy.
boolean
C0032961 (UMLS CUI [1])
lactation
Item
nursing mothers.
boolean
C0006147 (UMLS CUI [1])
claustrophobia
Item
subjects who are claustrophobic and are unable to tolerate mr imaging.
boolean
C0008909 (UMLS CUI [1])
creatinine
Item
patients with a serum creatinine concentration above 4mg/dl.
boolean
C0201976 (UMLS CUI [1])
bilateral renal stents
Item
bilateral renal stents.
boolean
C1322812 (UMLS CUI [1,1])
C0238767 (UMLS CUI [1,2])
dipstick urine test, bp, bun, creatinine
Item
healthy subjects must not have an abnormality detected on dipstick urinalysis, or a systolic bp above 140 mmhg or a diastolic bp above 90 mmhg on screening examination or an abnormal bun or creatinine level in the blood.
boolean
C0430370 (UMLS CUI [1])
C0005823 (UMLS CUI [2])
C0005845 (UMLS CUI [3])
C0201976 (UMLS CUI [4])

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