ID

36833

Description

LIPT - Liraglutide in Polycystic Ovary Syndrome; ODM derived from: https://clinicaltrials.gov/show/NCT02073929

Link

https://clinicaltrials.gov/show/NCT02073929

Keywords

  1. 6/13/19 6/13/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

June 13, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Polycystic Ovary Syndrome NCT02073929

Eligibility Polycystic Ovary Syndrome NCT02073929

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
pcos
Description

Polycystic Ovary Syndrome

Data type

boolean

Alias
UMLS CUI [1]
C0032460
>18 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
premenopausal
Description

Premenopausal state

Data type

boolean

Alias
UMLS CUI [1]
C0232969
bmi >25 og 25 and thereunder + insulin resistent
Description

Body mass index | Resistant to Insulin

Data type

boolean

Alias
UMLS CUI [1]
C1305855
UMLS CUI [2,1]
C0332325
UMLS CUI [2,2]
C0021641
exclusion criteria (including):
Description

Exclusion Criteria

Data type

boolean

Alias
UMLS CUI [1]
C0680251
actualt or intended pregnancy
Description

Pregnancy | Pregnancy, Planned

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
inadeqvat contraception
Description

Contraceptive methods Inadequate

Data type

boolean

Alias
UMLS CUI [1,1]
C0700589
UMLS CUI [1,2]
C0205412
hormonal contraception within 6 weeks
Description

Hormonal contraception

Data type

boolean

Alias
UMLS CUI [1]
C2985296
metfoomin, glp-1-analog or dpp iv inhibitor within 3 months
Description

Metformin | GLP-1 Analogue | Dipeptidyl-Peptidase IV Inhibitors

Data type

boolean

Alias
UMLS CUI [1]
C0025598
UMLS CUI [2]
C3273809
UMLS CUI [3]
C1827106
medications affectiv hemostatic mechanisme
Description

Hemostatic Agents

Data type

boolean

Alias
UMLS CUI [1]
C0019120
diabetes or other severe comorbidity
Description

Diabetes Mellitus | Comorbidity Severe

Data type

boolean

Alias
UMLS CUI [1]
C0011849
UMLS CUI [2,1]
C0009488
UMLS CUI [2,2]
C0205082
familar men
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
...
Description

Exclusion Criteria Additional

Data type

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C1524062

Similar models

Eligibility Polycystic Ovary Syndrome NCT02073929

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Polycystic Ovary Syndrome
Item
pcos
boolean
C0032460 (UMLS CUI [1])
Age
Item
>18 years
boolean
C0001779 (UMLS CUI [1])
Premenopausal state
Item
premenopausal
boolean
C0232969 (UMLS CUI [1])
Body mass index | Resistant to Insulin
Item
bmi >25 og 25 and thereunder + insulin resistent
boolean
C1305855 (UMLS CUI [1])
C0332325 (UMLS CUI [2,1])
C0021641 (UMLS CUI [2,2])
Exclusion Criteria
Item
exclusion criteria (including):
boolean
C0680251 (UMLS CUI [1])
Pregnancy | Pregnancy, Planned
Item
actualt or intended pregnancy
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Contraceptive methods Inadequate
Item
inadeqvat contraception
boolean
C0700589 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])
Hormonal contraception
Item
hormonal contraception within 6 weeks
boolean
C2985296 (UMLS CUI [1])
Metformin | GLP-1 Analogue | Dipeptidyl-Peptidase IV Inhibitors
Item
metfoomin, glp-1-analog or dpp iv inhibitor within 3 months
boolean
C0025598 (UMLS CUI [1])
C3273809 (UMLS CUI [2])
C1827106 (UMLS CUI [3])
Hemostatic Agents
Item
medications affectiv hemostatic mechanisme
boolean
C0019120 (UMLS CUI [1])
Diabetes Mellitus | Comorbidity Severe
Item
diabetes or other severe comorbidity
boolean
C0011849 (UMLS CUI [1])
C0009488 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Gender
Item
familar men
boolean
C0079399 (UMLS CUI [1])
Exclusion Criteria Additional
Item
...
boolean
C0680251 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])

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