ID
38530
Beschreibung
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
Stichworte
Versionen (2)
- 24.10.19 24.10.19 -
- 24.10.19 24.10.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
24. Oktober 2019
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY-NC 3.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Efficacy and Safety of GSK163090 in Subjects with Major Depressive Disorder; NCT00896363
End of Study
- StudyEvent: ODM
Beschreibung
Date of Visit/Assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-2
- C2985720
Beschreibung
Pharmacogenetic (PGx) Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0021430
- UMLS CUI-3
- C2349954
Beschreibung
Pharmacogenetic Test, Informed Consent, Withdraw
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2349954
Beschreibung
Pharmacogenetic Test, Informed Consent, Withdraw, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2349954
- UMLS CUI [1,4]
- C0011008
Beschreibung
Pharmacogenetic Test, Blood specimen, Destruction, Request
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
Beschreibung
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
- UMLS CUI [1,5]
- C0566251
Beschreibung
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
- UMLS CUI [1,5]
- C0566251
Beschreibung
Status of Treatment Blind
Alias
- UMLS CUI-1
- C2347038
- UMLS CUI-2
- C0449438
Beschreibung
Blinded Clinical Study, Subject Unblinding Event Record
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
Beschreibung
Blinded Clinical Study, Subject Unblinding Event Record, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0011008
Beschreibung
Blinded Clinical Study, Subject Unblinding Event Record, Reason and justification
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0566251
Beschreibung
Blinded Clinical Study, Subject Unblinding Event Record, Reason and justification
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0566251
Beschreibung
Medical Device Question
Alias
- UMLS CUI-1
- C0025080
- UMLS CUI-2
- C1522634
Beschreibung
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Beschreibung
Study Conclusion
Alias
- UMLS CUI-1
- C0008976
- UMLS CUI-2
- C1707478
Beschreibung
Completion Status, Date in time; Withdraw, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0805732
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [2,1]
- C2349954
- UMLS CUI [2,2]
- C0011008
Beschreibung
Patient withdrawn from trial
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0422727
Beschreibung
Patient withdrawn from trial, Reason and justification, Primary
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C0205225
Beschreibung
Patient withdrawn from trial, Reason and justification, Primary
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C0205225
Beschreibung
Clinical study case, Investigator Signature
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1706256
- UMLS CUI [1,2]
- C2346576
Ähnliche Modelle
End of Study
- StudyEvent: ODM
C1300638 (UMLS CUI [1,2])
C2985720 (UMLS CUI-2)
C2985720 (UMLS CUI [2])
C0021430 (UMLS CUI-2)
C2349954 (UMLS CUI-3)
C0021430 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0566251 (UMLS CUI [1,5])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0566251 (UMLS CUI [1,5])
C0449438 (UMLS CUI-2)
C3897431 (UMLS CUI [1,2])
C3897431 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C3897431 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C3897431 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C1522634 (UMLS CUI-2)
C1551358 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C2349954 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C0566251 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,3])
C2346576 (UMLS CUI [1,2])