Eligibility Diabetes Mellitus NCT01956851

Criteria
Descripción

Criteria

exclusion criteria-
Descripción

Exclusion Criteria

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0680251
patients of age group more than 45 yrs and below 25 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
pregnant or lactating or post menopausal females.
Descripción

Pregnancy | Breast Feeding | Postmenopausal state

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0232970
females with irregular menstrual cycles or galactorrhea
Descripción

Irregular periods

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0156404
patients on medications interfering with hormonal functions
Descripción

Pharmaceutical Preparations Interfere with Hormone function

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0682760
patients with history suggestive of gonadal dysfunction (hypogonadism primary or secondary)
Descripción

Suggestive of Gonadal Disorders | Primary hypogonadism | Secondary hypogonadism

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0332299
UMLS CUI [1,2]
C0018050
UMLS CUI [2]
C0948896
UMLS CUI [3]
C0271623
patients with polycystic ovarian disease (pcod)
Descripción

Polycystic Ovary Syndrome

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032460
patients with chronic kidney disease with gfr (glomerular filtration rate) <60ml/min
Descripción

Chronic Kidney Disease | Glomerular Filtration Rate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1561643
UMLS CUI [2]
C0017654
patients receiving gonadal therapy in the form of gnrh (gonadotropin-releasing hormone) agonist or antagonist, estrogen, progesterone or testosterone preparations
Descripción

Therapy Gonadal | Gonadotropin Releasing Hormone Agonist | Gonadotropin releasing hormone antagonist | Estrogens | Progesterone | Testosterone

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0018067
UMLS CUI [2]
C2267073
UMLS CUI [3]
C1268855
UMLS CUI [4]
C0014939
UMLS CUI [5]
C0033308
UMLS CUI [6]
C0039601
patients not willing to give informed consent
Descripción

Informed Consent Unwilling

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080

Similar models

Eligibility Diabetes Mellitus NCT01956851

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
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])
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])
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])
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])
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])
Informed Consent Unwilling
Item
patients not willing to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])