Informatie:
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ID
29038
Beschrijving
A Multi-Centre, Randomised, Double-Blind, Parallel-Group, Placebo- and Active-Controlled, Flexible Dose Study Evaluating the Efficacy, Safety and Tolerability of Extended-Release Bupropion Hydrochloride (150mg - 300mg once daily), Extended-Release Venlafaxine Hydrochloride (75mg - 150mg once daily) and Placebo in Subjects with Major Depressive Disorder
Trefwoorden
Versies (1)
- 21-02-18 21-02-18 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
21 februari 2018
DOI
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Licentie
Creative Commons BY-NC 3.0
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Study Evaluating Extended-Release Bupropion Hydrochloride and Extended-Release Venlafaxine Hydrochloride in Subjects with Major Depressive Disorder 101497
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Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Montgomery-Asberg Depression Rating Scale Questionnaire
Item
integer
C4054475 (UMLS CUI [1])
Hamilton Anxiety Rating Scale Questionnaire
Item
integer
C3541258 (UMLS CUI [1])
Clinical Global Impression
Item
boolean
C3639708 (UMLS CUI [1])
Sheehan Disability Scale Questionnaire
Item
Der Fragebogen Sheehan-Disability-Scale wurde bearbeitet.
integer
C3813719 (UMLS CUI [1])
Quality of life enjoyment and satisfaction questionaire - short form Q-LES-Q-SF
Item
boolean
C130318 (UMLS CUI [1])
Motivation and energy inventory - MEI
Item
integer
C3846158 (UMLS CUI [1])
C0449820 (UMLS CUI [2,1])
C0026605 (UMLS CUI [2,2])
C0449820 (UMLS CUI [2,1])
C0026605 (UMLS CUI [2,2])
Changes in sexual functioning questionaire
Item
text
C3846158 (UMLS CUI [1])
C0278092 (UMLS CUI [2,1])
C0205307 (UMLS CUI [2,2])
C1705241 (UMLS CUI [2,3])
C0278092 (UMLS CUI [2,1])
C0205307 (UMLS CUI [2,2])
C1705241 (UMLS CUI [2,3])
Date of assessment
Item
date
C2985720 (UMLS CUI [1])
Satisfaction with study medication
Item
float
C0242428 (UMLS CUI [1,1])
C0013216 (UMLS CUI [1,2])
C0013216 (UMLS CUI [1,2])
Weight
Item
float
C0005910 (UMLS CUI [1])
Heart rate
Item
integer
C0018810 (UMLS CUI [1])
Blood Pressure Systolic
Item
integer
C0871470 (UMLS CUI [1])
Diastolic blood pressure
Item
integer
C0428883 (UMLS CUI [1])
adverse events
Item
boolean
C0877248 (UMLS CUI [1])
concomitant medication changes
Item
boolean
C2347852 (UMLS CUI [1,1])
C2169461 (UMLS CUI [1,2])
C2169461 (UMLS CUI [1,2])
ECG completed
Item
boolean
C1623258 (UMLS CUI [1])
Date of ECG
Item
date
C2826640 (UMLS CUI [1])
ECG Finding
Item
boolean
C0438154 (UMLS CUI [1])
Date of blood sample
Item
date
C0005834 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
Date of urine samples
Item
date
C2371162 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
laboratory abnormalities
Item
boolean
C1853129 (UMLS CUI [1])
Serum hCG
Item
boolean
C2348195 (UMLS CUI [1])
Sample Date hCG
Item
date
C1302413 (UMLS CUI [1,1])
C2348195 (UMLS CUI [1,2])
C2348195 (UMLS CUI [1,2])
Serum hCG Result
Item
boolean
C2348195 (UMLS CUI [1])
Investigational Product
Item
boolean
C0304229 (UMLS CUI [1])
Research Comments
Item
text
C25704 (NCI Thesaurus ValueDomain)
C15319 (NCI Thesaurus ObjectClass)
C25393 (NCI Thesaurus Property)
C0947611 (UMLS CUI [1,1])
C0022885 (UMLS CUI [1,2])
C15319 (NCI Thesaurus ObjectClass)
C25393 (NCI Thesaurus Property)
C0947611 (UMLS CUI [1,1])
C0022885 (UMLS CUI [1,2])
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