Informationen:
Fehler:
ID
21143
Beschreibung
Randomized Trial Comparing N of 1 Trials to Standard Practice to Improve Adherence to Statins in Patients With Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00299169
Link
https://clinicaltrials.gov/show/NCT00299169
Stichworte
Versionen (1)
- 11.04.17 11.04.17 -
Hochgeladen am
11. April 2017
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Diabetes NCT00299169
Eligibility Diabetes NCT00299169
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Diabetes NCT00299169
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Diagnosis of Diabetes mellitus
Item
established diagnosis of type 1 or 2 diabetes
boolean
C0011900 (UMLS CUI [1,1])
C0011849 (UMLS CUI [1,2])
C0011849 (UMLS CUI [1,2])
Age
Item
age 18-80 years
boolean
C0001779 (UMLS CUI [1])
Indication for a statin
Item
indication for a statin by the 2003 canadian diabetes association (cda) clinical practice guidelines
boolean
C0360714 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,2])
Re-try statin therapy
Item
willingness to re-try a statin despite previous apparent intolerance
boolean
C0360714 (UMLS CUI [1,1])
C0205341 (UMLS CUI [1,2])
C0205341 (UMLS CUI [1,2])
Informed consent
Item
provision of signed informed consent
boolean
C0021430 (UMLS CUI [1])
Contraindication to statin
Item
contraindication to a statin: previous rhabdomyolysis, active liver disease or unexplained persistent elevations of serum transaminases (ck, ast, alt >three times upper limit of normal), pregnancy or lactation
boolean
C0522473 (UMLS CUI [1,1])
C0360714 (UMLS CUI [1,2])
C0360714 (UMLS CUI [1,2])
Creatinine clearance
Item
impaired renal function: severe renal insufficiency (creatinine clearance <30 ml/min)
boolean
C0373595 (UMLS CUI [1])
Life Expectancy
Item
presence of a condition such as malignancy for which the one-year prognosis is poor
boolean
C0023671 (UMLS CUI [1])
Compliance
Item
inability of the patient to comply with the rigorous conditions of the trial
boolean
C1321605 (UMLS CUI [1])
Comorbidity
Item
any other condition deemed to render the study harmful to the participant
boolean
C0009488 (UMLS CUI [1])