ID
38307
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)
- 09.10.19 09.10.19 -
- 24.10.19 24.10.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
9. Oktober 2019
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Efficacy and Safety of GSK163090 in Subjects with Major Depressive Disorder; NCT00896363
Common CRF : Meds Recorded at Home
- StudyEvent: ODM
Beschreibung
Meds Recorded at Home
Alias
- UMLS CUI-1
- C2347852
- UMLS CUI-2
- C0442519
Beschreibung
Concomitant Agent, Home environment, Sequence Number
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0442519
- UMLS CUI [1,3]
- C2348184
Beschreibung
Concomitant Agent, Home environment, Medication name
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0442519
- UMLS CUI [1,3]
- C2360065
Beschreibung
Concomitant Agent, Home environment, Medication name, Reported Term
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0442519
- UMLS CUI [1,3]
- C2360065
- UMLS CUI [1,4]
- C2826302
Beschreibung
Concomitant Agent, Home environment, Pharmaceutical Preparations, Synonym
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0442519
- UMLS CUI [1,3]
- C0013227
- UMLS CUI [1,4]
- C0871468
Beschreibung
Concomitant Agent, Home environment, Code
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0442519
- UMLS CUI [1,3]
- C0805701
Beschreibung
Concomitant Agent, Home environment, Code, Failed
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0442519
- UMLS CUI [1,3]
- C0805701
- UMLS CUI [1,4]
- C0231175
Beschreibung
Concomitant Agent, Home environment, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0442519
- UMLS CUI [1,3]
- C0011008
Beschreibung
Concomitant Agent, Home environment, Time
Datentyp
time
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0442519
- UMLS CUI [1,3]
- C0040223
Ähnliche Modelle
Common CRF : Meds Recorded at Home
- StudyEvent: ODM
C1300638 (UMLS CUI [1,2])
C0442519 (UMLS CUI-2)
C0442519 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
C0442519 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
C0442519 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
C2826302 (UMLS CUI [1,4])
C0442519 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C0871468 (UMLS CUI [1,4])
C0442519 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C0442519 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C0231175 (UMLS CUI [1,4])
C0442519 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0442519 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
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