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Information:
Fel:
ID
25535
Beskrivning
A Study to Compare the Effects of Exenatide and Sitagliptin on Postprandial Glucose in Subjects With Type 2 Diabetes Mellitus; ODM derived from: https://clinicaltrials.gov/show/NCT00477581
Länk
https://clinicaltrials.gov/show/NCT00477581
Nyckelord
Versioner (2)
- 2017-09-05 2017-09-05 -
- 2021-09-20 2021-09-20 -
Uppladdad den
5 september 2017
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Type 2 Diabetes Mellitus NCT00477581
Eligibility Type 2 Diabetes Mellitus NCT00477581
- StudyEvent: Eligibility
Similar models
Eligibility Type 2 Diabetes Mellitus NCT00477581
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Metformin
Item
treatment with metformin for at least 2 months
boolean
C0025598 (UMLS CUI [1])
Glycosylated hemoglobin A
Item
has hba1c 7.0% to 11.0%, inclusive, at screening
boolean
C0019018 (UMLS CUI [1])
Body mass index
Item
body mass index (bmi)25 kg/m^2 to 45 kg/m^2, inclusive
boolean
C1305855 (UMLS CUI [1])
Pharmaceutical Preparations Illicit | Therapeutic procedure Stable
Item
list of medications that are not allowed or the patient has been on stable treatment for at least 2 months:
boolean
C0013227 (UMLS CUI [1,1])
C0332266 (UMLS CUI [1,2])
C0087111 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
C0332266 (UMLS CUI [1,2])
C0087111 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
Hormone replacement therapy | Gender
Item
hormone replacement therapy (female subjects)
boolean
C0282402 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
C0079399 (UMLS CUI [2])
Gender Oral Contraceptives
Item
oral contraceptives (female subjects)
boolean
C0079399 (UMLS CUI [1,1])
C0009905 (UMLS CUI [1,2])
C0009905 (UMLS CUI [1,2])
Antihypertensive Agents
Item
antihypertensive agents
boolean
C0003364 (UMLS CUI [1])
Antilipemic agent
Item
lipid-lowering agents
boolean
C0003367 (UMLS CUI [1])
Thyroid hormone replacement therapy
Item
thyroid replacement therapy
boolean
C2242640 (UMLS CUI [1])
Exenatide | Byetta | Dipeptidyl-Peptidase IV Inhibitors
Item
has been treated with exenatide (byetta®) or any dpp-4 inhibitor prior to screening
boolean
C0167117 (UMLS CUI [1])
C1636686 (UMLS CUI [2])
C1827106 (UMLS CUI [3])
C1636686 (UMLS CUI [2])
C1827106 (UMLS CUI [3])
Investigational New Drugs | Study Subject Participation Status
Item
received any study medication or participated in any type of clinical trial within 30 days prior to screening
boolean
C0013230 (UMLS CUI [1])
C2348568 (UMLS CUI [2])
C2348568 (UMLS CUI [2])
Blood Donation | Blood Donation Planned
Item
has donated blood within 60 days of screening visit or is planning to donate blood during the study
boolean
C0005794 (UMLS CUI [1])
C0005794 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C0005794 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Pharmaceutical Preparations
Item
treated with any of the following medications:
boolean
C0013227 (UMLS CUI [1])
Sulfonylurea | Thiazolidinediones
Item
sulfonylurea or thiazolidinedione within 3 months of screening;
boolean
C0038766 (UMLS CUI [1])
C1257987 (UMLS CUI [2])
C1257987 (UMLS CUI [2])
alpha-Glucosidase Inhibitors | Meglitinide | nateglinide | Pramlintide | Symlin
Item
alpha-glucosidase inhibitor, meglitinide, nateglinide, or pramlintide (symlin®)within 30 days of screening;
boolean
C1299007 (UMLS CUI [1])
C0065880 (UMLS CUI [2])
C0903898 (UMLS CUI [3])
C0537551 (UMLS CUI [4])
C1174780 (UMLS CUI [5])
C0065880 (UMLS CUI [2])
C0903898 (UMLS CUI [3])
C0537551 (UMLS CUI [4])
C1174780 (UMLS CUI [5])
Insulin
Item
insulin within 2 weeks prior to screening or insulin for longer than 1 week within 6 months of screening;
boolean
C0021641 (UMLS CUI [1])
Pharmaceutical Preparations Affecting Gastrointestinal Motility | Anticholinergic Agents | Macrolide Antibiotics | Dopamine Antagonists | Opioids | Reglan | Metoclopramide
Item
drugs that directly affect gastrointestinal motility, including but not limited to, anticholinergics, macrolide antibiotics, dopamine antagonists, opioids, and reglan®(metoclopramide);
boolean
C0013227 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0017184 (UMLS CUI [1,3])
C0242896 (UMLS CUI [2])
C0003240 (UMLS CUI [3])
C0242702 (UMLS CUI [4])
C0242402 (UMLS CUI [5])
C0034977 (UMLS CUI [6])
C0025853 (UMLS CUI [7])
C0392760 (UMLS CUI [1,2])
C0017184 (UMLS CUI [1,3])
C0242896 (UMLS CUI [2])
C0003240 (UMLS CUI [3])
C0242702 (UMLS CUI [4])
C0242402 (UMLS CUI [5])
C0034977 (UMLS CUI [6])
C0025853 (UMLS CUI [7])
Systemic steroids Oral | Systemic steroids Intravenous | Systemic steroids Intramuscular | Inhaled steroids | Steroids Intrapulmonary | Advair | Systemic Absorption Rate High
Item
systemic corticosteroids by oral, intravenous, or intramuscular route; or potent, inhaled, or intrapulmonary (including advair®) steroids known to have a high rate of systemic absorption;
boolean
C2825233 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C2825233 (UMLS CUI [2,1])
C1522726 (UMLS CUI [2,2])
C2825233 (UMLS CUI [3,1])
C1556154 (UMLS CUI [3,2])
C2065041 (UMLS CUI [4])
C0038317 (UMLS CUI [5,1])
C1522224 (UMLS CUI [5,2])
C0965130 (UMLS CUI [6])
C3850076 (UMLS CUI [7,1])
C1521828 (UMLS CUI [7,2])
C0205250 (UMLS CUI [7,3])
C1527415 (UMLS CUI [1,2])
C2825233 (UMLS CUI [2,1])
C1522726 (UMLS CUI [2,2])
C2825233 (UMLS CUI [3,1])
C1556154 (UMLS CUI [3,2])
C2065041 (UMLS CUI [4])
C0038317 (UMLS CUI [5,1])
C1522224 (UMLS CUI [5,2])
C0965130 (UMLS CUI [6])
C3850076 (UMLS CUI [7,1])
C1521828 (UMLS CUI [7,2])
C0205250 (UMLS CUI [7,3])