Informações:
Falhas:
ID
38834
Descrição
Lifestyle Modification for Type 2 Diabetes Involving Reduction of After-meal Blood Glucose Elevations; ODM derived from: https://clinicaltrials.gov/show/NCT02432391
Link
https://clinicaltrials.gov/show/NCT02432391
Palavras-chave
Versões (1)
- 07/11/2019 07/11/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
7 de novembro de 2019
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Diabetes Mellitus, Type 2 NCT02432391
Eligibility Diabetes Mellitus, Type 2 NCT02432391
- StudyEvent: Eligibility
Similar models
Eligibility Diabetes Mellitus, Type 2 NCT02432391
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Non-Insulin-Dependent Diabetes Mellitus Disease length
Item
diagnosed with type 2 diabetes within the past 5 years
boolean
C0011860 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C0872146 (UMLS CUI [1,2])
Age
Item
age >24 and <80 years
boolean
C0001779 (UMLS CUI [1])
Hemoglobin A1c measurement
Item
hba1c >7.0%
boolean
C0474680 (UMLS CUI [1])
Participation Approved By Primary Care Physician
Item
approval of primary care physician to participate
boolean
C0679823 (UMLS CUI [1,1])
C1706842 (UMLS CUI [1,2])
C0033131 (UMLS CUI [1,3])
C1706842 (UMLS CUI [1,2])
C0033131 (UMLS CUI [1,3])
Hypoglycemic Agents | Insulin | Sulfonylureas | Glinides | Dipeptidyl-Peptidase IV Inhibitors
Item
currently using, or used within the last 3 months, medications that directly lower bg (e.g., insulin, sulfonylureas, glinides, or dpp-4 inhibitors).
boolean
C0020616 (UMLS CUI [1])
C0021641 (UMLS CUI [2])
C0038766 (UMLS CUI [3])
C3537178 (UMLS CUI [4])
C1827106 (UMLS CUI [5])
C0021641 (UMLS CUI [2])
C0038766 (UMLS CUI [3])
C3537178 (UMLS CUI [4])
C1827106 (UMLS CUI [5])
Thiazides More Than Hydrochlorothiazide Dose | Loop Diuretics More Than Furosemide Dose
Item
currently using, or used within the last 3 months, thiazides at doses above hctz 25 mg or equivalent, or loop diuretics above furosemide 20mg or equivalent.
boolean
C0541746 (UMLS CUI [1,1])
C0439093 (UMLS CUI [1,2])
C0020261 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,4])
C0354100 (UMLS CUI [2,1])
C0439093 (UMLS CUI [2,2])
C0016860 (UMLS CUI [2,3])
C0178602 (UMLS CUI [2,4])
C0439093 (UMLS CUI [1,2])
C0020261 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,4])
C0354100 (UMLS CUI [2,1])
C0439093 (UMLS CUI [2,2])
C0016860 (UMLS CUI [2,3])
C0178602 (UMLS CUI [2,4])
Pregnancy | Pregnancy, Planned
Item
currently pregnant or contemplating pregnancy in the coming year
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
C0032992 (UMLS CUI [2])
Pharmaceutical Preparations Preventing Weight loss | Prednisone
Item
currently using, or used within the last 3 months, medications that impede weight loss (e.g., prednisone)
boolean
C0013227 (UMLS CUI [1,1])
C1292733 (UMLS CUI [1,2])
C1262477 (UMLS CUI [1,3])
C0032952 (UMLS CUI [2])
C1292733 (UMLS CUI [1,2])
C1262477 (UMLS CUI [1,3])
C0032952 (UMLS CUI [2])
Condition Excludes Increased physical activity | Neuropathy Severe | Cardiovascular Disease | Emphysema | Osteoarthritis | Cerebrovascular accident
Item
having conditions that preclude increasing physical activity, e.g. severe neuropathy, active cardiovascular disease, emphysema, osteoarthritis, stroke.
boolean
C0348080 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C4039165 (UMLS CUI [1,3])
C0442874 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0007222 (UMLS CUI [3])
C0034067 (UMLS CUI [4])
C0029408 (UMLS CUI [5])
C0038454 (UMLS CUI [6])
C0332196 (UMLS CUI [1,2])
C4039165 (UMLS CUI [1,3])
C0442874 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0007222 (UMLS CUI [3])
C0034067 (UMLS CUI [4])
C0029408 (UMLS CUI [5])
C0038454 (UMLS CUI [6])
Cancer treatment
Item
undergoing cancer treatment
boolean
C0920425 (UMLS CUI [1])
Acidosis, Lactic
Item
history of lactic acidosis
boolean
C0001125 (UMLS CUI [1])
Renal Insufficiency
Item
diagnosed with renal impairment
boolean
C1565489 (UMLS CUI [1])