Informatie:
Fout:
ID
39301
Beschrijving
Cohort Study to Evaluate Ovarian Function; ODM derived from: https://clinicaltrials.gov/show/NCT02294500
Link
https://clinicaltrials.gov/show/NCT02294500
Trefwoorden
Versies (1)
- 17-12-19 17-12-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
17 december 2019
DOI
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Licentie
Creative Commons BY 4.0
Model Commentaren :
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Eligibility Female Infertility Due to Diminished Ovarian Reserve NCT02294500
Eligibility Female Infertility Due to Diminished Ovarian Reserve NCT02294500
- StudyEvent: Eligibility
Similar models
Eligibility Female Infertility Due to Diminished Ovarian Reserve NCT02294500
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Karnofsky Performance Status
Item
karnofsky performance statue ≥ 70,
boolean
C0206065 (UMLS CUI [1])
White Blood Cell Count procedure
Item
wbc > 3,000/mm³,
boolean
C0023508 (UMLS CUI [1])
Hemoglobin measurement
Item
hb > 9.0g/dl,
boolean
C0518015 (UMLS CUI [1])
Platelet Count measurement
Item
platelet > 100,000 /mm³,
boolean
C0032181 (UMLS CUI [1])
Aspartate aminotransferase measurement | Alanine aminotransferase measurement
Item
sgot/sgpt < 60 iu/l,
boolean
C0201899 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
C0201836 (UMLS CUI [2])
Serum total bilirubin measurement
Item
t-bil < 1.5 mg/dl,
boolean
C1278039 (UMLS CUI [1])
Creatinine measurement, serum
Item
cr < 1.2 mg/dl,
boolean
C0201976 (UMLS CUI [1])
PaO2
Item
pao2 > 80 torr,
boolean
C0202155 (UMLS CUI [1])
ECG normal
Item
normal ecg,
boolean
C0522054 (UMLS CUI [1])
Informed Consent
Item
written informed consent.
boolean
C0021430 (UMLS CUI [1])
Patients Uninformed
Item
patients without information,
boolean
C0030705 (UMLS CUI [1,1])
C0562357 (UMLS CUI [1,2])
C0562357 (UMLS CUI [1,2])
Risk factors Clinical
Item
clinical risk factors,
boolean
C0035648 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,2])
Communicable Disease
Item
patients who have active infection.
boolean
C0009450 (UMLS CUI [1])