ID
33649
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 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
Mots-clés
Versions (1)
- 18/12/2018 18/12/2018 -
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
GP Response
- StudyEvent: ODM
Description
GP Response
Alias
- UMLS CUI-1
- C0017319
- UMLS CUI-2
- C1706817
Description
*Recent = dated within 12 months of the first dose administration
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0332185
- UMLS CUI [1,2]
- C0017319
- UMLS CUI [1,3]
- C1706817
Description
If no, exclude
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2348568
- UMLS CUI [1,2]
- C3900053
Description
Comments
Type de données
text
Alias
- UMLS CUI [1]
- C0947611
Description
Conclusion
Alias
- UMLS CUI-1
- C1707478
Similar models
GP Response
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0017319 (UMLS CUI [1,2])
C1706817 (UMLS CUI [1,3])
C3900053 (UMLS CUI [1,2])
C0031831 (UMLS CUI [1,2])