ID

38832

Beschrijving

Variation of Glucose Values at Early Stages of Diabetes - Continuous Glucose Monitoring; ODM derived from: https://clinicaltrials.gov/show/NCT02294370

Link

https://clinicaltrials.gov/show/NCT02294370

Trefwoorden

Versies (1)
  1. 07-11-19 07-11-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

7 november 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Diabetes Mellitus, Type 2 NCT02294370

Engels

Eligibility Diabetes Mellitus, Type 2 NCT02294370

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
individuals with impaired glucose tolerance (2h plasma glucose during oral glucose tolerance test >7.8-11.1 mmol/l, n=50) or with type 2 diabetes (fasting plasma glucose > 7.0 mmol/l and/or 2h plasma glucose > 11.1 mmol/l on two occasions, or both criteria fulfilled in the same oral glucose tolerance test while not pregnant, n=50) with short duration (<3 years); 40 from padova university hospital, 60 from the botnia study or the ppp (prevalence, prediction, prevention)-botnia study in finland.
Beschrijving

Decreased glucose tolerance | Plasma Glucose Measurement Oral Glucose Tolerance Test | Diabetes Mellitus, Non-Insulin-Dependent | Plasma fasting glucose measurement | Pregnancy Absent

Datatype

boolean

Alias
UMLS CUI [1]
C0151671
UMLS CUI [2,1]
C0202042
UMLS CUI [2,2]
C0029161
UMLS CUI [3]
C0011860
UMLS CUI [4]
C0583513
UMLS CUI [5,1]
C0032961
UMLS CUI [5,2]
C0332197
age 40-75 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
medication with: insulin, glucagon-like peptide-1 (glp-1)-analogues, sulphonylureas, oral corticosteroids, thyreostatic agents or thyroid hormone, luteinizing-hormone-releasing hormone (lhrh) analogues
Beschrijving

Insulin | GLP-1 Analogue | Sulfonylurea | Adrenal Cortex Hormones Oral | Thyreostatic therapy | Thyroid Hormones | LH-RH Analogs

Datatype

boolean

Alias
UMLS CUI [1]
C0021641
UMLS CUI [2]
C3273809
UMLS CUI [3]
C0038766
UMLS CUI [4,1]
C0001617
UMLS CUI [4,2]
C1527415
UMLS CUI [5]
C1696471
UMLS CUI [6]
C0040135
UMLS CUI [7]
C1518041
pregnancy
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
known changes in retinal fundus photographs
Beschrijving

Change Ophthalmoscopy Retinal

Datatype

boolean

Alias
UMLS CUI [1,1]
C0392747
UMLS CUI [1,2]
C0029090
UMLS CUI [1,3]
C0035298
known, microalbuminuria
Beschrijving

Microalbuminuria

Datatype

boolean

Alias
UMLS CUI [1]
C0730345
hba1c >8%
Beschrijving

Hemoglobin A1c measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0474680
fasting plasma glucose >10 mmol/l
Beschrijving

Plasma fasting glucose measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0583513
medication with metformin, glitazones, gliptins (or acarbose) is allowed but gliptins and acarbose need to be stopped 2 days before testing and during the study
Beschrijving

Metformin allowed | Thiazolidinediones allowed | Gliptins To be stopped | Acarbose To be stopped

Datatype

boolean

Alias
UMLS CUI [1,1]
C0025598
UMLS CUI [1,2]
C0683607
UMLS CUI [2,1]
C1257987
UMLS CUI [2,2]
C0683607
UMLS CUI [3,1]
C1827106
UMLS CUI [3,2]
C1272691
UMLS CUI [4,1]
C0050393
UMLS CUI [4,2]
C1272691
Terug naar het begin van de pagina

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT02294370

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Decreased glucose tolerance | Plasma Glucose Measurement Oral Glucose Tolerance Test | Diabetes Mellitus, Non-Insulin-Dependent | Plasma fasting glucose measurement | Pregnancy Absent
Item
individuals with impaired glucose tolerance (2h plasma glucose during oral glucose tolerance test >7.8-11.1 mmol/l, n=50) or with type 2 diabetes (fasting plasma glucose > 7.0 mmol/l and/or 2h plasma glucose > 11.1 mmol/l on two occasions, or both criteria fulfilled in the same oral glucose tolerance test while not pregnant, n=50) with short duration (<3 years); 40 from padova university hospital, 60 from the botnia study or the ppp (prevalence, prediction, prevention)-botnia study in finland.
boolean
C0151671 (UMLS CUI [1])
C0202042 (UMLS CUI [2,1])
C0029161 (UMLS CUI [2,2])
C0011860 (UMLS CUI [3])
C0583513 (UMLS CUI [4])
C0032961 (UMLS CUI [5,1])
C0332197 (UMLS CUI [5,2])
Age
Item
age 40-75 years
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Insulin | GLP-1 Analogue | Sulfonylurea | Adrenal Cortex Hormones Oral | Thyreostatic therapy | Thyroid Hormones | LH-RH Analogs
Item
medication with: insulin, glucagon-like peptide-1 (glp-1)-analogues, sulphonylureas, oral corticosteroids, thyreostatic agents or thyroid hormone, luteinizing-hormone-releasing hormone (lhrh) analogues
boolean
C0021641 (UMLS CUI [1])
C3273809 (UMLS CUI [2])
C0038766 (UMLS CUI [3])
C0001617 (UMLS CUI [4,1])
C1527415 (UMLS CUI [4,2])
C1696471 (UMLS CUI [5])
C0040135 (UMLS CUI [6])
C1518041 (UMLS CUI [7])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Change Ophthalmoscopy Retinal
Item
known changes in retinal fundus photographs
boolean
C0392747 (UMLS CUI [1,1])
C0029090 (UMLS CUI [1,2])
C0035298 (UMLS CUI [1,3])
Microalbuminuria
Item
known, microalbuminuria
boolean
C0730345 (UMLS CUI [1])
Hemoglobin A1c measurement
Item
hba1c >8%
boolean
C0474680 (UMLS CUI [1])
Plasma fasting glucose measurement
Item
fasting plasma glucose >10 mmol/l
boolean
C0583513 (UMLS CUI [1])
Metformin allowed | Thiazolidinediones allowed | Gliptins To be stopped | Acarbose To be stopped
Item
medication with metformin, glitazones, gliptins (or acarbose) is allowed but gliptins and acarbose need to be stopped 2 days before testing and during the study
boolean
C0025598 (UMLS CUI [1,1])
C0683607 (UMLS CUI [1,2])
C1257987 (UMLS CUI [2,1])
C0683607 (UMLS CUI [2,2])
C1827106 (UMLS CUI [3,1])
C1272691 (UMLS CUI [3,2])
C0050393 (UMLS CUI [4,1])
C1272691 (UMLS CUI [4,2])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial