ID
17029
Description
A Phase 2, Double-Blind, Randomized, Placebo and Active-Controlled Dose-Finding Study to Assess the Efficacy, Safety and Tolerability of Multiple Oral Doses of ASP1941 in Subjects with Type 2 Diabetes MellitusTEST Study Cumulative
Mots-clés
Versions (2)
- 22/08/2016 22/08/2016 -
- 28/09/2016 28/09/2016 -
Téléchargé le
22 août 2016
DOI
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Licence
Creative Commons BY-NC 3.0 Legacy
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DM-ASP1941-1941-CL-0004 NCT01071850
Cumulative DM-ASP1941-1941-CL-0004 NCT01071850
- StudyEvent: ODM
Description
Medical History
Alias
- UMLS CUI-1
- C0262926
Description
medical Condition, past or present
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0332119
Description
Medical Condition
Type de données
text
Alias
- UMLS CUI [1]
- C0012634
Description
Onset Date Medical Condition
Type de données
date
Alias
- UMLS CUI [1,1]
- C0574845
- UMLS CUI [1,2]
- C0012634
Description
Medical Condition Ongoing
Type de données
boolean
Alias
- UMLS CUI [1]
- C0012634
Description
Recovery
Type de données
date
Alias
- UMLS CUI [1]
- C2004454
Description
Medication
Type de données
boolean
Alias
- UMLS CUI [1]
- C0013227
Description
Concomitant Medication
Alias
- UMLS CUI-1
- C2347852
Description
Concomitant Medication
Type de données
boolean
Alias
- UMLS CUI [1]
- C2347852
Description
Medication
Type de données
text
Alias
- UMLS CUI [1]
- C2347852
- UMLS CUI [2]
- C0013227
Description
Route of administration
Type de données
integer
Alias
- UMLS CUI [1]
- C0013153
- UMLS CUI [2]
- C2347852
Description
Start date
Type de données
date
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0808070
Description
StopDate
Type de données
date
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0011008
Description
Ongoing
Type de données
boolean
Alias
- UMLS CUI [1]
- C2347852
Description
Dose
Type de données
text
Alias
- UMLS CUI [1]
- C3174092
- UMLS CUI [2]
- C2347852
Description
Dose Units
Type de données
text
Alias
- UMLS CUI [1]
- C3174092
- UMLS CUI [2]
- C2347852
Description
Frequency
Type de données
text
Alias
- UMLS CUI [1]
- C3476109
- UMLS CUI [2]
- C2347852
Description
Indication
Type de données
text
Alias
- UMLS CUI [1]
- C3146298
- UMLS CUI [2]
- C2347852
Description
Reason
Type de données
integer
Alias
- UMLS CUI [1]
- C0392360
- UMLS CUI [2]
- C2347852
Description
Adverse Events
Alias
- UMLS CUI-1
- C0877248
Description
Adverse Events
Type de données
boolean
Alias
- UMLS CUI [1]
- C0877248
Description
Adverse Event
Type de données
text
Alias
- UMLS CUI [1]
- C0877248
Description
Adverse Event Onset Date
Type de données
date
Alias
- UMLS CUI [1]
- C2985916
Description
Adverse Event Onset Date
Type de données
integer
Alias
- UMLS CUI [1]
- C2985916
Description
Adverse Event End Date
Type de données
date
Alias
- UMLS CUI [1]
- C2697886
Description
Adverse Event Outcome
Type de données
integer
Alias
- UMLS CUI [1]
- C1705586
Description
Adverse Event Course
Type de données
integer
Alias
- UMLS CUI [1]
- C0877248
Description
Adverse Event Severity
Type de données
integer
Alias
- UMLS CUI [1]
- C1710066
Description
Serious Adverse Event
Type de données
boolean
Alias
- UMLS CUI [1]
- C1519255
Description
Serious Adverse Event
Type de données
text
Alias
- UMLS CUI [1]
- C1519255
Description
AE Death
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2]
- C0011065
Description
AE Hospital
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2]
- C0019993
Description
AE Congenital
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2]
- C2826727
Description
AE Life threatening
Type de données
integer
Alias
- UMLS CUI [1]
- C1517874
Description
AE persistent
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2]
- C0231170
Description
AE Other
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2]
- C0205394
Description
Study treatment
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2]
- C0949266
Description
Treatment required
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0877248
- UMLS CUI [1,3]
- C0087111
- UMLS CUI [1,4]
- C1521801
Description
Drug Treatment required
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2]
- C0013216
Description
Non Medication Therapy
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
Description
AE Relation to study drug
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C0304229
Description
AE UTI/Genital
Type de données
integer
Alias
- UMLS CUI [1]
- C0877248
- UMLS CUI [2]
- C0729552
- UMLS CUI [3]
- C0042029
Description
AE UTI/Genital
Type de données
integer
Alias
- UMLS CUI [1]
- C0877248
- UMLS CUI [2]
- C0729552
- UMLS CUI [3]
- C0042029
- UMLS CUI [4]
- C3244125
Description
AE hypoglycemia
Type de données
integer
Alias
- UMLS CUI [1]
- C0877248
- UMLS CUI [2]
- C0020615
Description
AE hypoglycemia glucometer
Type de données
boolean
Alias
- UMLS CUI [1]
- C0877248
- UMLS CUI [2]
- C0020615
- UMLS CUI [3]
- C0472226
Description
AE hypoglycemia glucometer
Type de données
text
Unités de mesure
- mmol/L
Alias
- UMLS CUI [1]
- C0877248
- UMLS CUI [2]
- C0020615
- UMLS CUI [3]
- C0472226
- UMLS CUI [4]
- C0005802
Description
AE hypoglycemia last meal
Type de données
text
Unités de mesure
- hours
Alias
- UMLS CUI [1]
- C0877248
- UMLS CUI [2]
- C0020615
Description
AE hypoglycemia last meal
Type de données
text
Unités de mesure
- hours
Alias
- UMLS CUI [1]
- C0877248
- UMLS CUI [2]
- C0020615
- UMLS CUI [3]
- C0013216
Description
AE hypoglycemia last meal
Type de données
text
Unités de mesure
- hours
Alias
- UMLS CUI [1]
- C0877248
- UMLS CUI [2]
- C0020615
- UMLS CUI [3]
- C0013216
Description
Serious Adverse Event
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
Description
Adjudication Reference ID
Type de données
text
Alias
- UMLS CUI [1]
- C0680730
Description
Hospitalization Records
Alias
- UMLS CUI-1
- C0019993
Description
Hospitalization
Type de données
boolean
Alias
- UMLS CUI [1]
- C0019993
Description
Date of admission
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0019993
Description
Ongoing
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0549178
- UMLS CUI [1,2]
- C0019993
Description
Date of Discharge
Type de données
date
Alias
- UMLS CUI [1,1]
- C2361123
- UMLS CUI [1,2]
- C0019993
Description
Type of Hospitalization
Type de données
integer
Alias
- UMLS CUI [1]
- C0019993
Description
Reason for Hospitalization
Type de données
integer
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2]
- C0019993
Description
Reason for Hospitalization, Other
Type de données
text
Alias
- UMLS CUI [1]
- C0019993
- UMLS CUI [2]
- C0205394
Similar models
Cumulative DM-ASP1941-1941-CL-0004 NCT01071850
- StudyEvent: ODM
C0262926 (UMLS CUI [1,2])
C0332119 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2])
C2347852 (UMLS CUI [2])
C0808070 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C2347852 (UMLS CUI [2])
C2347852 (UMLS CUI [2])
C2347852 (UMLS CUI [2])
C2347852 (UMLS CUI [2])
C0019993 (UMLS CUI [2])
C0231170 (UMLS CUI [2])
C0949266 (UMLS CUI [2])
C0877248 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C1521801 (UMLS CUI [1,4])
C0013216 (UMLS CUI [2])
C0877248 (UMLS CUI [2,1])
C0304229 (UMLS CUI [2,2])
C0729552 (UMLS CUI [2])
C0042029 (UMLS CUI [3])
C0729552 (UMLS CUI [2])
C0042029 (UMLS CUI [3])
C3244125 (UMLS CUI [4])
C0020615 (UMLS CUI [2])
C0020615 (UMLS CUI [2])
C0472226 (UMLS CUI [3])
C0020615 (UMLS CUI [2])
C0472226 (UMLS CUI [3])
C0005802 (UMLS CUI [4])
C0020615 (UMLS CUI [2])
C0020615 (UMLS CUI [2])
C0013216 (UMLS CUI [3])
C0020615 (UMLS CUI [2])
C0013216 (UMLS CUI [3])
C0019993 (UMLS CUI [1,2])
C0019993 (UMLS CUI [1,2])
C0019993 (UMLS CUI [1,2])
C0019993 (UMLS CUI [2])
C0205394 (UMLS CUI [2])
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