ID
17580
Beschrijving
NCT00428090 / GSK-AVA105640 A 24-week, double-blind, double-dummy, randomized, parallel-group study to investigate the effects of rosiglitazone (extended release tablets), donepezil, and placebo as monotherapy on cognition and overall clinical response in APOE e4-stratified subjects with mild to moderate Alzheimer’s disease. (REFLECT-1)
Trefwoorden
Versies (1)
- 25-09-16 25-09-16 -
Geüploaded op
25 september 2016
DOI
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Licentie
Creative Commons BY-NC-ND 3.0
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REFLECT-1 Visit 7 NCT00428090
REFLECT-1 Visit 7 NCT00428090
- StudyEvent: ODM
Beschrijving
Investigator Instructions
Alias
- UMLS CUI-1
- C1442085
Beschrijving
Subject Continuation
Alias
- UMLS CUI-1
- C0805733
Beschrijving
Subject Continuation
Datatype
text
Alias
- UMLS CUI [1]
- C0805733
Beschrijving
Vital signs
Alias
- UMLS CUI-1
- C0518766
Beschrijving
Weight
Datatype
float
Maateenheden
- kg
Alias
- UMLS CUI [1]
- C0005910
Beschrijving
Systolic Blood Pressure
Datatype
float
Maateenheden
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Beschrijving
Diastolic Blood Pressure
Datatype
float
Maateenheden
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Beschrijving
Patient Position
Datatype
boolean
Alias
- UMLS CUI [1]
- C0449850
Beschrijving
Heart Rate
Datatype
float
Maateenheden
- Beats/Min
Alias
- UMLS CUI [1]
- C0018810
Beschrijving
Central Laboratory (Non Fasting Samples)
Alias
- UMLS CUI-1
- C1880016
Beschrijving
Concomitant medication
Alias
- UMLS CUI-1
- C2347852
Beschrijving
Adverse Event
Alias
- UMLS CUI-1
- C0877248
Beschrijving
Adverse Event
Datatype
text
Alias
- UMLS CUI [1]
- C0877248
Beschrijving
Physical Examination
Alias
- UMLS CUI-1
- C0031809
Beschrijving
Physical Examination
Datatype
text
Alias
- UMLS CUI [1]
- C0031809
Beschrijving
Pedal Oedema
Alias
- UMLS CUI-1
- C0574002
Beschrijving
Pedal Oedema: depth
Datatype
text
Alias
- UMLS CUI [1,1]
- C0574002
- UMLS CUI [1,2]
- C0205125
Beschrijving
Pedal Oedema: Site
Datatype
text
Alias
- UMLS CUI [1,1]
- C0574002
- UMLS CUI [1,2]
- C1515974
Beschrijving
Investigational Product - dispense (for Visit 3: Weeks 5 - 8; for Visit 4: Weeks 9 -16; for Visit 5: weeks 17 - 24) study medication as specified by the IVRS system. Record start date, container number and number of tablets dispensed below (stop date and tablets returned will be completed when the bottle is returned)
Alias
- UMLS CUI-1
- C0304229
Beschrijving
Investigational Product
Datatype
text
Alias
- UMLS CUI [1]
- C0304229
Beschrijving
Start Date
Datatype
date
Maateenheden
- dd/MMM/yy
Alias
- UMLS CUI [1]
- C0808070
Beschrijving
Stop Date
Datatype
date
Maateenheden
- dd/MMM/yy
Alias
- UMLS CUI [1]
- C0806020
Beschrijving
Dose
Datatype
float
Maateenheden
- mg
Alias
- UMLS CUI [1]
- C3174092
Beschrijving
IP Container No.
Datatype
float
Alias
- UMLS CUI [1]
- C0180098
Beschrijving
Discontinuation
Datatype
boolean
Alias
- UMLS CUI [1]
- C0457454
Beschrijving
Compliance - dispense (for Visit 3: Weeks 5 - 8; for Visit 4: Weeks 9 -16; for Visit 5: weeks 17 - 24) study medication as specified by the IVRS system. Record start date, container number and number of tablets dispensed below (stop date and tablets returned will be completed when the bottle is returned)
Alias
- UMLS CUI-1
- C1321605
Beschrijving
End of Visit Reminder
Alias
- UMLS CUI-1
- C1709896
- UMLS CUI-2
- C1320303
Similar models
REFLECT-1 Visit 7 NCT00428090
- StudyEvent: ODM
C0205125 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])
C1320303 (UMLS CUI [1,2])