ID

36833

Description

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

Lien

https://clinicaltrials.gov/show/NCT02073929

Mots-clés

  1. 13/06/2019 13/06/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

13 juin 2019

DOI

Pour une demande vous connecter.

Licence

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

Type de données

boolean

Alias
UMLS CUI [1]
C0032460
>18 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
premenopausal
Description

Premenopausal state

Type de données

boolean

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

Body mass index | Resistant to Insulin

Type de données

boolean

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

Exclusion Criteria

Type de données

boolean

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

Pregnancy | Pregnancy, Planned

Type de données

boolean

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

Contraceptive methods Inadequate

Type de données

boolean

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

Hormonal contraception

Type de données

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

Type de données

boolean

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

Hemostatic Agents

Type de données

boolean

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

Diabetes Mellitus | Comorbidity Severe

Type de données

boolean

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

Gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
...
Description

Exclusion Criteria Additional

Type de données

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)
Type de données
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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