ID
33645
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 the result of the physical examination. It should be filled out at screening visit and updated throughout the study if necessary. 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)
- 01/12/2018 01/12/2018 -
- 09/12/2018 09/12/2018 -
- 18/12/2018 18/12/2018 - Sarah Riepenhausen
Détendeur de droits
GlaxoSmithKline
Téléchargé le
18 décembre 2018
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
Physical Examination
- StudyEvent: ODM
Description
Physical Examination
Alias
- UMLS CUI-1
- C0031809
Description
Examination
Type de données
text
Alias
- UMLS CUI [1]
- C0031809
Description
Examination Result
Type de données
text
Alias
- UMLS CUI [1,1]
- C0031809
- UMLS CUI [1,2]
- C1274040
Description
Examination Result Abnormal
Type de données
text
Alias
- UMLS CUI [1,1]
- C0031809
- UMLS CUI [1,2]
- C1274040
- UMLS CUI [1,3]
- C0205161
Description
Examination Result Clinically Significant
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0459424
- UMLS CUI [1,2]
- C2826634
Description
Conclusion
Alias
- UMLS CUI-1
- C1707478
Similar models
Physical Examination
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,3])
C2826634 (UMLS CUI [1,2])
C0031831 (UMLS CUI [1,2])
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