ID

38777

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

  1. 03-11-19 03-11-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

3 november 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Efficacy and Safety of GSK163090 in Subjects with Major Depressive Disorder; NCT00896363

CRB Electronic Signature Affidavit

CRB Electronic Signature Affidavit
Beschrijving

CRB Electronic Signature Affidavit

Alias
UMLS CUI-1
C2346576
By my dated signature below, I, (First Name) (Last Name) verify that this case report form accurately displays the results of the examinations, tests, evaluations and treatments performed on this patient.
Beschrijving

Investigator Name

Datatype

text

Alias
UMLS CUI [1]
C2826892
Date
Beschrijving

Investigator Signature, Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C2346576
UMLS CUI [1,2]
C0011008
Investigator Signature
Beschrijving

Investigator Signature

Datatype

text

Alias
UMLS CUI [1]
C2346576

Similar models

CRB Electronic Signature Affidavit

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
CRB Electronic Signature Affidavit
C2346576 (UMLS CUI-1)
Investigator Name
Item
By my dated signature below, I, (First Name) (Last Name) verify that this case report form accurately displays the results of the examinations, tests, evaluations and treatments performed on this patient.
text
C2826892 (UMLS CUI [1])
Investigator Signature, Date in time
Item
Date
date
C2346576 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Investigator Signature
Item
Investigator Signature
text
C2346576 (UMLS CUI [1])

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial