ID

33686

Description

Efficacy of Insulin Lispro Mix 50/50 Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT01303042

Link

https://clinicaltrials.gov/show/NCT01303042

Keywords

  1. 12/19/18 12/19/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

December 19, 2018

DOI

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License

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 2 NCT01303042

Eligibility Diabetes Mellitus, Type 2 NCT01303042

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes patients who are treated with insulin basal/bolus therapy ( long-acting insulin at bedtime and mealtime rapid-acting insulin ) or analog insulin therapy t.i.d. (including therapies with aspart mix 70/30 and lispro mix 75/25) and whose hba1c is above 7.4%.
Description

Diabetes Mellitus, Non-Insulin-Dependent | Insulin regime Basal | Insulin regime Bolus | Long-Acting Insulin Bedtime | Short-Acting Insulin Mealtime | Insulin Analog | Insulin Aspart | Insulin Lispro | Hemoglobin A1c measurement

Data type

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2,1]
C0557978
UMLS CUI [2,2]
C0205112
UMLS CUI [3,1]
C0557978
UMLS CUI [3,2]
C1705509
UMLS CUI [4,1]
C0304870
UMLS CUI [4,2]
C0521112
UMLS CUI [5,1]
C0356365
UMLS CUI [5,2]
C0587119
UMLS CUI [6]
C2825028
UMLS CUI [7]
C1708521
UMLS CUI [8]
C0293359
UMLS CUI [9]
C0474680
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with renal failure with serum creatinine level ≧ 2.0
Description

Kidney Failure | Creatinine measurement, serum

Data type

boolean

Alias
UMLS CUI [1]
C0035078
UMLS CUI [2]
C0201976
patients with hepatocirrhosis
Description

Liver Cirrhosis

Data type

boolean

Alias
UMLS CUI [1]
C0023890
patients with proliferative diabetic retinopathy or worse
Description

Proliferative diabetic retinopathy

Data type

boolean

Alias
UMLS CUI [1]
C0154830
patients with acute infectious disease
Description

Communicable Disease

Data type

boolean

Alias
UMLS CUI [1]
C0009450
patients who are treated with steroids
Description

Steroid therapy

Data type

boolean

Alias
UMLS CUI [1]
C0149783
patients with cancer
Description

Malignant Neoplasms

Data type

boolean

Alias
UMLS CUI [1]
C0006826
pregnant patients
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
patients who are decided to be inappropriate subjects by study physicians
Description

Study Subject Participation Status Inappropriate

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT01303042

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent | Insulin regime Basal | Insulin regime Bolus | Long-Acting Insulin Bedtime | Short-Acting Insulin Mealtime | Insulin Analog | Insulin Aspart | Insulin Lispro | Hemoglobin A1c measurement
Item
type 2 diabetes patients who are treated with insulin basal/bolus therapy ( long-acting insulin at bedtime and mealtime rapid-acting insulin ) or analog insulin therapy t.i.d. (including therapies with aspart mix 70/30 and lispro mix 75/25) and whose hba1c is above 7.4%.
boolean
C0011860 (UMLS CUI [1])
C0557978 (UMLS CUI [2,1])
C0205112 (UMLS CUI [2,2])
C0557978 (UMLS CUI [3,1])
C1705509 (UMLS CUI [3,2])
C0304870 (UMLS CUI [4,1])
C0521112 (UMLS CUI [4,2])
C0356365 (UMLS CUI [5,1])
C0587119 (UMLS CUI [5,2])
C2825028 (UMLS CUI [6])
C1708521 (UMLS CUI [7])
C0293359 (UMLS CUI [8])
C0474680 (UMLS CUI [9])
Item Group
C0680251 (UMLS CUI)
Kidney Failure | Creatinine measurement, serum
Item
patients with renal failure with serum creatinine level ≧ 2.0
boolean
C0035078 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Liver Cirrhosis
Item
patients with hepatocirrhosis
boolean
C0023890 (UMLS CUI [1])
Proliferative diabetic retinopathy
Item
patients with proliferative diabetic retinopathy or worse
boolean
C0154830 (UMLS CUI [1])
Communicable Disease
Item
patients with acute infectious disease
boolean
C0009450 (UMLS CUI [1])
Steroid therapy
Item
patients who are treated with steroids
boolean
C0149783 (UMLS CUI [1])
Malignant Neoplasms
Item
patients with cancer
boolean
C0006826 (UMLS CUI [1])
Pregnancy
Item
pregnant patients
boolean
C0032961 (UMLS CUI [1])
Study Subject Participation Status Inappropriate
Item
patients who are decided to be inappropriate subjects by study physicians
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])

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