Informations:
Erreur:
ID
12917
Description
ADPKD Cohort Study; ODM derived from: https://clinicaltrials.gov/show/NCT02084849
Lien
https://clinicaltrials.gov/show/NCT02084849
Mots-clés
Versions (1)
- 06/01/2016 06/01/2016 -
Détendeur de droits
CC BY-NC 3.0
Téléchargé le
6 janvier 2016
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
Modèle Commentaires :
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Eligibility Autosomal Dominant Polycystic Kidney Disease NCT02084849
Eligibility Autosomal Dominant Polycystic Kidney Disease NCT02084849
- StudyEvent: Eligibility
Similar models
Eligibility Autosomal Dominant Polycystic Kidney Disease NCT02084849
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
group 1
Item
group 1
boolean
hypertension
Item
hypertension diagnosed early in the course of the disease (less than 25 years for men; less than 30 years for women)
boolean
C0020538 (UMLS CUI [1])
adpkd
Item
adpkd diagnosed in utero or in the first year of life
boolean
C0085413 (UMLS CUI [1])
proteinuria
Item
the presence of proteinuria (between 180 mg and 1 gm/day) without evidence of a second renal disorder
boolean
C0033687 (UMLS CUI [1])
Pregnancy
Item
a history of more than 3 pregnancies and hypertension
boolean
C0032961 (UMLS CUI [1])
hematuria
Item
a history of gross hematuria
boolean
C0018965 (UMLS CUI [1])
creatinine
Item
a serum creatinine concentration less than 1.4 mg/dl
boolean
C0201976 (UMLS CUI [1])
more than 10 cysts
Item
adpkd diagnosed in childhood with more than 10 cysts
boolean
C0085413 (UMLS CUI [1])
group 2
Item
group 2
boolean
creatinine 2
Item
serum creatinine concentration >1.4 and
boolean
C0201976 (UMLS CUI [1])
renal length
Item
renal length greater than 15 cm and
boolean
C1444754 (UMLS CUI [1])
age
Item
age less than 60 years of age
boolean
C0001779 (UMLS CUI [1])
severe pain or discomfort
Item
severe pain or discomfort as assessed by the primary care physician related to adpkd
boolean
C0030193 (UMLS CUI [1])
reliable follow-up
Item
subjects, who in the assessment of the principal investigator cannot provide reliable follow-up
boolean
C1321605 (UMLS CUI [1])
iothalamate
Item
subjects who cannot be exposed to iothalamate
boolean
C0022032 (UMLS CUI [1])
mri
Item
subjects who cannot undergo mri due to the presence of a pacemaker or surgical clip in the abdomen
boolean
C0024485 (UMLS CUI [1])
life expectancy
Item
subjects who are not anticipated to survive during the duration of the study (e.g. underlying malignancy)
boolean
C0023671 (UMLS CUI [1])
informed consent
Item
subjects who cannot provide informed consent
boolean
C0021430 (UMLS CUI [1])
pregnancy
Item
women who are pregnant or who have undergone a pregnancy in the last 6 months or who are presently breastfeeding
boolean
C0032961 (UMLS CUI [1])
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