Informatie:
Fout:
ID
33677
Beschrijving
Association of Kisspeptin Levels With Insulin Secretion in Diabetes Mellitus; ODM derived from: https://clinicaltrials.gov/show/NCT01956851
Link
https://clinicaltrials.gov/show/NCT01956851
Trefwoorden
Versies (1)
- 19-12-18 19-12-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
19 december 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Diabetes Mellitus NCT01956851
Eligibility Diabetes Mellitus NCT01956851
- StudyEvent: Eligibility
Similar models
Eligibility Diabetes Mellitus NCT01956851
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Exclusion Criteria
Item
exclusion criteria-
boolean
C0680251 (UMLS CUI [1])
Age
Item
patients of age group more than 45 yrs and below 25 years
boolean
C0001779 (UMLS CUI [1])
Pregnancy | Breast Feeding | Postmenopausal state
Item
pregnant or lactating or post menopausal females.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0232970 (UMLS CUI [3])
C0006147 (UMLS CUI [2])
C0232970 (UMLS CUI [3])
Irregular periods
Item
females with irregular menstrual cycles or galactorrhea
boolean
C0156404 (UMLS CUI [1])
Pharmaceutical Preparations Interfere with Hormone function
Item
patients on medications interfering with hormonal functions
boolean
C0013227 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0682760 (UMLS CUI [1,3])
C0521102 (UMLS CUI [1,2])
C0682760 (UMLS CUI [1,3])
Suggestive of Gonadal Disorders | Primary hypogonadism | Secondary hypogonadism
Item
patients with history suggestive of gonadal dysfunction (hypogonadism primary or secondary)
boolean
C0332299 (UMLS CUI [1,1])
C0018050 (UMLS CUI [1,2])
C0948896 (UMLS CUI [2])
C0271623 (UMLS CUI [3])
C0018050 (UMLS CUI [1,2])
C0948896 (UMLS CUI [2])
C0271623 (UMLS CUI [3])
Polycystic Ovary Syndrome
Item
patients with polycystic ovarian disease (pcod)
boolean
C0032460 (UMLS CUI [1])
Chronic Kidney Disease | Glomerular Filtration Rate
Item
patients with chronic kidney disease with gfr (glomerular filtration rate) <60ml/min
boolean
C1561643 (UMLS CUI [1])
C0017654 (UMLS CUI [2])
C0017654 (UMLS CUI [2])
Therapy Gonadal | Gonadotropin Releasing Hormone Agonist | Gonadotropin releasing hormone antagonist | Estrogens | Progesterone | Testosterone
Item
patients receiving gonadal therapy in the form of gnrh (gonadotropin-releasing hormone) agonist or antagonist, estrogen, progesterone or testosterone preparations
boolean
C0087111 (UMLS CUI [1,1])
C0018067 (UMLS CUI [1,2])
C2267073 (UMLS CUI [2])
C1268855 (UMLS CUI [3])
C0014939 (UMLS CUI [4])
C0033308 (UMLS CUI [5])
C0039601 (UMLS CUI [6])
C0018067 (UMLS CUI [1,2])
C2267073 (UMLS CUI [2])
C1268855 (UMLS CUI [3])
C0014939 (UMLS CUI [4])
C0033308 (UMLS CUI [5])
C0039601 (UMLS CUI [6])
Informed Consent Unwilling
Item
patients not willing to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,2])