ID

38306

Beschrijving

Study ID: 109035 Clinical Study ID: 109035 Study Title: A Randomised, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy and Safety of GSK163090 in Subjects With Major Depressive Disorder Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00896363 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GSK163090 1 mg, GSK163090 Placebo, GSK163090 3 mg Trade Name: Study Indication: Depressive Disorder

Trefwoorden

Versies (2)
  1. 09-10-19 09-10-19 -
  2. 24-10-19 24-10-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

9 oktober 2019

DOI

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Licentie

Creative Commons BY-NC 3.0
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Efficacy and Safety of GSK163090 in Subjects with Major Depressive Disorder; NCT00896363

Engels

Common CRF : Drug Dispensing/Return Information

1 Formulieren  
Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
Site
Beschrijving

Study Site

Datatype

text

Alias
UMLS CUI [1]
C2825164
Patient
Beschrijving

Patient name

Datatype

text

Alias
UMLS CUI [1]
C1299487
Patient No
Beschrijving

Patients, Identification number

Datatype

integer

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1300638
Drug Dispensing/Return Information
Beschrijving

Drug Dispensing/Return Information

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C0947323
UMLS CUI-3
C0332156
Container dispensed at
Beschrijving

Experimental drug, Dispensing medication, Containers

Datatype

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0947323
UMLS CUI [1,3]
C0180098
Date dispensed
Beschrijving

Experimental drug, Dispensing medication, Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0947323
UMLS CUI [1,3]
C0011008
Investigational product container number
Beschrijving

Experimental drug, Containers, Numbers

Datatype

integer

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0180098
UMLS CUI [1,3]
C0237753
Terug naar het begin van de pagina

Similar models

Common CRF : Drug Dispensing/Return Information

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Study Site
Item
Site
text
C2825164 (UMLS CUI [1])
Patient name
Item
Patient
text
C1299487 (UMLS CUI [1])
Patients, Identification number
Item
Patient No
integer
C0030705 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
Item Group
Drug Dispensing/Return Information
C0304229 (UMLS CUI-1)
C0947323 (UMLS CUI-2)
C0332156 (UMLS CUI-3)
Experimental drug, Dispensing medication, Containers
Item
Container dispensed at
text
C0304229 (UMLS CUI [1,1])
C0947323 (UMLS CUI [1,2])
C0180098 (UMLS CUI [1,3])
Experimental drug, Dispensing medication, Date in time
Item
Date dispensed
date
C0304229 (UMLS CUI [1,1])
C0947323 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Experimental drug, Containers, Numbers
Item
Investigational product container number
integer
C0304229 (UMLS CUI [1,1])
C0180098 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])
Terug naar het begin van de pagina 

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