ID
33649
Descripción
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 informations about the response of the subjects general practicioner. It should be filled out at the first treatment period. Only include this form if a recent GP response is required before dosing. 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
Palabras clave
Versiones (1)
- 18/12/18 18/12/18 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
18 de diciembre de 2018
DOI
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Licencia
Creative Commons BY-NC 3.0
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Effect of Lamictal on Resting Motor Threshold Study-ID 107434
GP Response
- StudyEvent: ODM
Descripción
GP Response
Alias
- UMLS CUI-1
- C0017319
- UMLS CUI-2
- C1706817
Descripción
*Recent = dated within 12 months of the first dose administration
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0332185
- UMLS CUI [1,2]
- C0017319
- UMLS CUI [1,3]
- C1706817
Descripción
If no, exclude
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2348568
- UMLS CUI [1,2]
- C3900053
Descripción
Comments
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0947611
Descripción
Conclusion
Alias
- UMLS CUI-1
- C1707478
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GP Response
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