ID
33266
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 any unscheduled blood sampling for pharmakokinetics. It should be filled out at follow up visit. It should be filled out at each visit, if any unscheduled blood samples for pharmacogenetics had been taken. 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 (3)
- 3/12/18 3/12/18 -
- 19/12/18 19/12/18 -
- 9/1/19 9/1/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
3 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
Unscheduled Blood Sampling for PK
- StudyEvent: ODM
Descripción
Blood Sample for PK and metabolites
Alias
- UMLS CUI-1
- C0005834
- UMLS CUI-2
- C0031327
- UMLS CUI-3
- C0870883
Descripción
Date
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0011008
Descripción
Time
Tipo de datos
time
Alias
- UMLS CUI [1]
- C0040223
Descripción
enter one code only: 1 = Slow/blocked cannula 2 = poor veins/difficult venepuncture 3 = subject not in attendance 4 = Other (enter comment)
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C3854240
- UMLS CUI [1,3]
- C0200345
Descripción
Sample Number
Tipo de datos
text
Descripción
PK sample type number
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0201734
- UMLS CUI [1,2]
- C1299222
Descripción
Clinical Staff Initials
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2986440
- UMLS CUI [1,2]
- C0871685
Descripción
Conclusion
Alias
- UMLS CUI-1
- C1707478
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- StudyEvent: ODM
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C0200345 (UMLS CUI [1,3])
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