ID
34781
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 contains information about any recorded neurological abnormalities during the study. It should be filled out at screening and anytime an additional neurological examination is performed.
Mots-clés
Versions (2)
- 05/12/2018 05/12/2018 -
- 28/01/2019 28/01/2019 - Sarah Riepenhausen
Détendeur de droits
GlaxoSmithKline
Téléchargé le
28 janvier 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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Effect of Lamictal on Resting Motor Threshold Study-ID 107434
Neurological Examination Record
- StudyEvent: ODM
Description
Neurological Examination
Alias
- UMLS CUI-1
- C0027853
Description
Only necessary for additional neurological examinations.
Type de données
boolean
Alias
- UMLS CUI [1]
- C0027853
Description
Only necessary for additional neurological examinations.
Type de données
text
Alias
- UMLS CUI [1,1]
- C2986440
- UMLS CUI [1,2]
- C1552089
Description
Date of Assessment
Type de données
date
Alias
- UMLS CUI [1]
- C2985720
Description
Neurological Examination Results
Alias
- UMLS CUI-1
- C1274040
- UMLS CUI-2
- C0027853
Description
Neurological Examination
Type de données
text
Alias
- UMLS CUI [1]
- C0027853
Description
Neurological Examination Finding
Type de données
text
Alias
- UMLS CUI [1,1]
- C0027853
- UMLS CUI [1,2]
- C0243095
Description
Comments
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Description
Neurological Examination Conclusion
Alias
- UMLS CUI-1
- C0027853
- UMLS CUI-2
- C1707478
Description
For Screening: If NO, the subject is not eligible to participate in the study. For additional examinations: If no, comment.
Type de données
boolean
Alias
- UMLS CUI [1]
- C1112287
Description
Only relevant for additional examinations.
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Description
Physician's Initials
Type de données
text
Alias
- UMLS CUI [1,1]
- C2986440
- UMLS CUI [1,2]
- C0031831
Similar models
Neurological Examination Record
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,2])
C1552089 (UMLS CUI [1,2])
C0027853 (UMLS CUI-2)
C0243095 (UMLS CUI [1,2])
C1707478 (UMLS CUI-2)
C0031831 (UMLS CUI [1,2])
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