ID
34732
Description
Study ID: 107434 Clinical Study ID: NAP107434 Study Title: A randomised, double-blind, double-dummy, placebo controlled, three-way cross-over study to investigate the effect of single oral doses of 100 mg GW273225 (4030W92) and 325 mg LAMICTAL on resting motor threshold in healthy subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Study Link: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GW273225 Trade Name: lamictal Study Indication: Bipolar Disorder This form is for documentation of the transcranial magnetic stimulation (TMS). TMS assessment to be performed in triplicate. The measurements are to be performed within 10 minutes of each other. It should be filled out at each treatment period. Screening Visit: 28 days prior to first dosing. Treatment Period: The day before dosing, until 48h after dosing. Follow-Up: 14-21 days after last dose
Mots-clés
Versions (3)
- 03/12/2018 03/12/2018 -
- 21/01/2019 21/01/2019 -
- 25/01/2019 25/01/2019 - Sarah Riepenhausen
Détendeur de droits
GlaxoSmithKline
Téléchargé le
25 janvier 2019
DOI
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Licence
Creative Commons BY-NC 3.0
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Effect of Lamictal on Resting Motor Threshold Study-ID 107434
TMS Form (Treatment Periods)
- StudyEvent: ODM
Description
Rest Transcranial Magnetic Stimulation
Alias
- UMLS CUI-1
- C0013806
- UMLS CUI-2
- C0436548
Description
Protocol Time
Type de données
text
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C2348563
Description
Study Day
Type de données
text
Description
Date of Assessment
Type de données
date
Alias
- UMLS CUI [1]
- C2985720
Description
Assessment
Type de données
integer
Alias
- UMLS CUI [1]
- C0199171
Description
Actual Time
Type de données
time
Alias
- UMLS CUI [1]
- C0040223
Description
Motor Threshold
Type de données
integer
Unités de mesure
- %
Alias
- UMLS CUI [1,1]
- C0026606
- UMLS CUI [1,2]
- C0449864
Description
If No, comment
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0205197
- UMLS CUI [1,2]
- C0436548
- UMLS CUI [1,3]
- C0035253
Description
Comments
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Description
Active Transcranial Magnetic Stimulation
Alias
- UMLS CUI-1
- C0013806
- UMLS CUI-2
- C0436548
Description
Protocol Time
Type de données
text
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C2348563
Description
Study Day
Type de données
text
Description
Date of Assessment
Type de données
date
Alias
- UMLS CUI [1]
- C2985720
Description
Assessment
Type de données
integer
Alias
- UMLS CUI [1]
- C0199171
Description
Actual Time
Type de données
time
Alias
- UMLS CUI [1]
- C0040223
Description
Motor Threshold
Type de données
integer
Unités de mesure
- %
Alias
- UMLS CUI [1,1]
- C0026606
- UMLS CUI [1,2]
- C0449864
Description
If No, comment
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0205197
- UMLS CUI [1,2]
- C0436548
- UMLS CUI [1,3]
- C0205177
Description
Comments
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Description
Conclusion
Alias
- UMLS CUI-1
- C1707478
Description
Protocol Time
Type de données
text
Alias
- UMLS CUI [1]
- C0439564
Description
Assessor Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1552089
- UMLS CUI [1,2]
- C0600091
Description
TMS Machine Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0436548
- UMLS CUI [1,2]
- C0336779
- UMLS CUI [1,3]
- C0600091
Description
Neurophysiologist Staff Initials
Type de données
text
Alias
- UMLS CUI [1,1]
- C1552089
- UMLS CUI [1,2]
- C2986440
- UMLS CUI [1,3]
- C0586861
Similar models
TMS Form (Treatment Periods)
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0436548 (UMLS CUI-2)
C0449864 (UMLS CUI [1,2])
C0436548 (UMLS CUI [1,2])
C0035253 (UMLS CUI [1,3])
C0436548 (UMLS CUI-2)
C0449864 (UMLS CUI [1,2])
C0436548 (UMLS CUI [1,2])
C0205177 (UMLS CUI [1,3])
C0600091 (UMLS CUI [1,2])
C0336779 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C2986440 (UMLS CUI [1,2])
C0586861 (UMLS CUI [1,3])