ID
31480
Description
Study ID: 105012 Clinical Study ID: NSS105012 Study Title: Emotional processing in healthy male volunteers treated with GSK424887. A single centre, randomised, double-blind, placebo-controlled parallel group study Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01424384 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GSK424887 Trade Name: Citalopram Study Indication: Depressive Disorder and Anxiety Disorders
Mots-clés
Versions (2)
- 27/08/2018 27/08/2018 -
- 20/09/2021 20/09/2021 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
27 août 2018
DOI
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Licence
Creative Commons BY-NC 3.0
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Emotional processing in healthy male volunteers treated with GSK424887 NCT01424384
Logs and Repeats and Concomitant Medications
- StudyEvent: ODM
Description
Adverse Event/ Concomitant medication/ Repeat assessment check questions
Alias
- UMLS CUI-1
- C0877248
- UMLS CUI-2
- C2826666
- UMLS CUI-3
- C0220825
Description
Pharmaceutical Preparations Concomitant Therapy; Concomitant Medications; Study; During
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1707479
- UMLS CUI [1,3]
- C2603343
- UMLS CUI [1,4]
- C0347984
Description
Non-serious Adverse Event; Study; During
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2603343
- UMLS CUI [1,3]
- C0347984
Description
Serious Adverse Event; Study; During
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2603343
- UMLS CUI [1,3]
- C0347984
Description
Hematologic Tests; Blood sample taken; Repeat | Chemistry, Clinical; Specimen Collection; Repeat
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0018941
- UMLS CUI [1,2]
- C1277698
- UMLS CUI [1,3]
- C0205341
- UMLS CUI [2,1]
- C0008000
- UMLS CUI [2,2]
- C0200345
- UMLS CUI [2,3]
- C0205341
Description
Urinalysis; Specimen Collection; Repeat
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0205341
Description
Electrocardiogram; Repeat
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0013798
- UMLS CUI [1,2]
- C0205341
Description
ECG abnormality; Clinically Significant Indicator
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1832603
- UMLS CUI [1,2]
- C2985739
Description
Vital signs; Repeat
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0205341
Description
Blood sample taken; Drug Kinetics; Repeat
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1277698
- UMLS CUI [1,2]
- C0031327
- UMLS CUI [1,3]
- C0205341
Description
Holter Electrocardiography; Repeat
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0013801
- UMLS CUI [1,2]
- C0205341
Description
Holter Electrocardiography; Electrocardiogram abnormal; Clinically Significant Indicator
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0013801
- UMLS CUI [1,2]
- C0522055
- UMLS CUI [1,3]
- C2985739
Description
Concomitant Medications
Alias
- UMLS CUI-1
- C0013227
- UMLS CUI-2
- C1707479
Description
Pharmaceutical Preparations; Concomitant Therapy; Sequence Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1707479
- UMLS CUI [1,3]
- C2348184
Description
Medication name
Type de données
text
Alias
- UMLS CUI [1]
- C2360065
Description
Concomitant Medication Dose Unit
Type de données
float
Alias
- UMLS CUI [1]
- C2826646
Description
Unit
Type de données
integer
Alias
- UMLS CUI [1]
- C0439148
Description
Medication frequency
Type de données
integer
Alias
- UMLS CUI [1]
- C3476109
Description
Drug Administration Routes
Type de données
integer
Alias
- UMLS CUI [1]
- C0013153
Description
Concomitant Medication Use Indication
Type de données
text
Alias
- UMLS CUI [1]
- C2826696
Description
Concomitant Medication Start Date | Pharmaceutical Preparations; Concomitant Therapy; Start time
Type de données
datetime
Alias
- UMLS CUI [1]
- C2826734
- UMLS CUI [2,1]
- C0013227
- UMLS CUI [2,2]
- C1707479
- UMLS CUI [2,3]
- C1301880
Description
Pharmaceutical Preparations; Concomitant Therapy; Study; Before
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C1707479
- UMLS CUI [1,3]
- C2603343
- UMLS CUI [1,4]
- C0332152
Description
Concomitant Medication Ongoing
Type de données
boolean
Alias
- UMLS CUI [1]
- C2826666
Description
Concomitant Medication End Date | Pharmaceutical Preparations; Concomitant Therapy; End Time
Type de données
datetime
Alias
- UMLS CUI [1]
- C2826744
- UMLS CUI [2,1]
- C0013227
- UMLS CUI [2,2]
- C1707479
- UMLS CUI [2,3]
- C1522314
Similar models
Logs and Repeats and Concomitant Medications
- StudyEvent: ODM
C2985720 (UMLS CUI-2)
C2985720 (UMLS CUI [1,2])
C2826666 (UMLS CUI-2)
C0220825 (UMLS CUI-3)
C1707479 (UMLS CUI [1,2])
C2603343 (UMLS CUI [1,3])
C0347984 (UMLS CUI [1,4])
C2603343 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,3])
C2603343 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,3])
C1277698 (UMLS CUI [1,2])
C0205341 (UMLS CUI [1,3])
C0008000 (UMLS CUI [2,1])
C0200345 (UMLS CUI [2,2])
C0205341 (UMLS CUI [2,3])
C0200345 (UMLS CUI [1,2])
C0205341 (UMLS CUI [1,3])
C0205341 (UMLS CUI [1,2])
C2985739 (UMLS CUI [1,2])
C0205341 (UMLS CUI [1,2])
C0031327 (UMLS CUI [1,2])
C0205341 (UMLS CUI [1,3])
C0205341 (UMLS CUI [1,2])
C0522055 (UMLS CUI [1,2])
C2985739 (UMLS CUI [1,3])
C1707479 (UMLS CUI-2)
C1707479 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
C0013227 (UMLS CUI [2,1])
C1707479 (UMLS CUI [2,2])
C1301880 (UMLS CUI [2,3])
C1707479 (UMLS CUI [1,2])
C2603343 (UMLS CUI [1,3])
C0332152 (UMLS CUI [1,4])
C0013227 (UMLS CUI [2,1])
C1707479 (UMLS CUI [2,2])
C1522314 (UMLS CUI [2,3])