Informationen:
Fehler:
ID
35765
Beschreibung
Effect of Paired Testing to Poorly Controlled Chinese Diabetes on Glycemic Control and Self Care; ODM derived from: https://clinicaltrials.gov/show/NCT02225691
Link
https://clinicaltrials.gov/show/NCT02225691
Stichworte
Versionen (1)
- 21.03.19 21.03.19 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
21. März 2019
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Diabetes Mellitus, Type 2 NCT02225691
Eligibility Diabetes Mellitus, Type 2 NCT02225691
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Diabetes Mellitus, Type 2 NCT02225691
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Diabetes Mellitus
Item
diagnosed with diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Hemoglobin A1c measurement
Item
hba1c ≥ 8% measured within the a month prior to enrolment
boolean
C0474680 (UMLS CUI [1])
Blood Glucose Self-Monitoring Regular Absent
Item
have not been performing smbg on a regular (daily) basis within the 3 months prior to enrolment
boolean
C0005803 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0205272 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Use of Accu-Chek Glucose Control Willing | Blood Glucose Self-Monitoring Daily Willing
Item
willing and able to use accu-chek® active blood glucose meter to perform daily smbg
boolean
C1524063 (UMLS CUI [1,1])
C0724912 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
C0005803 (UMLS CUI [2,1])
C0332173 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
C0724912 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
C0005803 (UMLS CUI [2,1])
C0332173 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Questionnaires Completion
Item
willing and able to complete participant questionnaires
boolean
C0034394 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,2])
Physician Visits
Item
willing and able to visit the physician at month 3 and month 6
boolean
C0031831 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,2])
Informed Consent
Item
provide informed consent prior to enrolling in the study
boolean
C0021430 (UMLS CUI [1])
Retinal Disease Requirement Light Coagulation | Retinal Disease Requirement Operation on retina
Item
any retinopathy that required photocoagulation or retinal surgery in the 6 months prior to enrolment or that may require photocoagulation or retinal surgery during the study
boolean
C0035309 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0023694 (UMLS CUI [1,3])
C0035309 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0197770 (UMLS CUI [2,3])
C1514873 (UMLS CUI [1,2])
C0023694 (UMLS CUI [1,3])
C0035309 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0197770 (UMLS CUI [2,3])
Medical condition Hospitalization Required | Elective Surgical Procedures
Item
any clinically significant condition that required hospitalization in the last 2 months prior to enrolment or that may require hospitalization (e.g. elective surgery) during the study
boolean
C3843040 (UMLS CUI [1,1])
C1708385 (UMLS CUI [1,2])
C0206058 (UMLS CUI [2])
C1708385 (UMLS CUI [1,2])
C0206058 (UMLS CUI [2])
Psychotic Disorders | Impaired cognition
Item
any clinically significant psychosis or cognitive impairment
boolean
C0033975 (UMLS CUI [1])
C0338656 (UMLS CUI [2])
C0338656 (UMLS CUI [2])
Compliance behavior Unlikely | Completion of clinical trial Unlikely
Item
unlikelihood to comply or complete the study
boolean
C1321605 (UMLS CUI [1,1])
C0750558 (UMLS CUI [1,2])
C2732579 (UMLS CUI [2,1])
C0750558 (UMLS CUI [2,2])
C0750558 (UMLS CUI [1,2])
C2732579 (UMLS CUI [2,1])
C0750558 (UMLS CUI [2,2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
women who are pregnant, lactating or planning to become pregnant during the study period
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])