Informatie:
Fout:
ID
32854
Beschrijving
A Study to Test the Safety and Efficacy of Adding Sitagliptin in Patients With Type 2 Diabetes Mellitus (MK0431-074); ODM derived from: https://clinicaltrials.gov/show/NCT00813995
Link
https://clinicaltrials.gov/show/NCT00813995
Trefwoorden
Versies (1)
- 16-11-18 16-11-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
16 november 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Type 2 Diabetes Mellitus NCT00813995
Eligibility Type 2 Diabetes Mellitus NCT00813995
- StudyEvent: Eligibility
Similar models
Eligibility Type 2 Diabetes Mellitus NCT00813995
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
18 - 78 years of age
boolean
C0001779 (UMLS CUI [1])
Metformin
Item
currently on metformin monotherapy
boolean
C0025598 (UMLS CUI [1])
Diabetes Mellitus, Insulin-Dependent | Ketoacidosis
Item
history of type 1 diabetes mellitus or ketoacidosis
boolean
C0011854 (UMLS CUI [1])
C0220982 (UMLS CUI [2])
C0220982 (UMLS CUI [2])
Weight Reduction Programs | Maintenance Phase Absent | Weight-Loss Agents
Item
currently on a weight loss program and not in the maintenance phase or has started on a weight loss medication within the last 8 weeks
boolean
C3179079 (UMLS CUI [1])
C0024501 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C0376606 (UMLS CUI [3])
C0024501 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C0376606 (UMLS CUI [3])
Operative Surgical Procedure Requirement General Anesthesia | Major surgery Planned
Item
has undergone surgery requiring general anesthesia within the past 4 weeks or has planned major surgery
boolean
C0543467 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0002915 (UMLS CUI [1,3])
C0679637 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C1514873 (UMLS CUI [1,2])
C0002915 (UMLS CUI [1,3])
C0679637 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
currently participating in a study or has participated in a study with or without an investigational compound or device within the past 12 weeks
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
Liver disease | Hepatitis B, Chronic | Hepatitis C, Chronic | Liver Cirrhosis | Gall Bladder Disease Symptomatic
Item
history of active liver disease such as chronic active hepatitis b or c, cirrhosis or symptomatic gallbladder disease
boolean
C0023895 (UMLS CUI [1])
C0524909 (UMLS CUI [2])
C0524910 (UMLS CUI [3])
C0023890 (UMLS CUI [4])
C0016977 (UMLS CUI [5,1])
C0231220 (UMLS CUI [5,2])
C0524909 (UMLS CUI [2])
C0524910 (UMLS CUI [3])
C0023890 (UMLS CUI [4])
C0016977 (UMLS CUI [5,1])
C0231220 (UMLS CUI [5,2])
HIV Seropositivity
Item
hiv positive
boolean
C0019699 (UMLS CUI [1])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
pregnant, breast-feeding or planning to become pregnant during the study
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Recreational drug use | Illicit medication use | Substance Use Disorders | Substance Dependence
Item
user of recreational or illicit drugs or has a recent history (within the past year) of drug or alcohol abuse or dependence
boolean
C0013146 (UMLS CUI [1])
C0281875 (UMLS CUI [2])
C0038586 (UMLS CUI [3])
C0038580 (UMLS CUI [4])
C0281875 (UMLS CUI [2])
C0038586 (UMLS CUI [3])
C0038580 (UMLS CUI [4])