ID
29790
Descripción
Study ID: 101464 Clinical Study ID: SCA101464 Study Title: A Multicenter, Randomized, Double-Blind, Parallel Group Study to Evaluate the Efficacy and Safety of a Flexible Dose of Lamotrigine Compared to Placebo as an Adjunctive Therapy to an Atypical Antipsychotic Agent(s) in Subjects with Schizophrenia Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00086593 https://clinicaltrials.gov/ct2/show/NCT00086593 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: lamotrigine Study Indication: Lamictal XR,Lamictal,LAMICTIN This ODM form contains Week 15 - Visit 13: 7-Day Follow-up.
Link
https://clinicaltrials.gov/ct2/show/NCT00086593
Palabras clave
Versiones (1)
- 19/4/18 19/4/18 - Sarah Riepenhausen
Titular de derechos de autor
GlaxoSmithKline
Subido en
19 de abril de 2018
DOI
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Licencia
Creative Commons BY-NC 3.0
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Evaluation of a Flexible Dose of Lamotrigine Compared to Placebo as an Adjunctive to Atypical Antipsychotic Agents in Schizophrenia NCT00086593
Week 15 - Visit 13: 7-Day Follow-up
- StudyEvent: ODM
Descripción
Pregnancy Test
Alias
- UMLS CUI-1
- C0430056
Descripción
Pregnancy Test applicable
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0032976
- UMLS CUI [1,2]
- C1706839
Descripción
Pregnancy test performed
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0032976
- UMLS CUI [1,2]
- C0884358
Descripción
If positive, complete PREGNANCY NOTIFICATION FORM.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0032976
- UMLS CUI [1,2]
- C1274040
Descripción
Pharmacokinetic Sampling
Descripción
Sample No.: BLD007
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0178913
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0201734
Descripción
Sampling Time
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0005834
- UMLS CUI [1,3]
- C0201734
Descripción
Sample No.: BLD007
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0201734
Descripción
Atypical Antipsychotic Dosing
Alias
- UMLS CUI-1
- C0040615
- UMLS CUI-2
- C0205182
- UMLS CUI-3
- C0178602
Descripción
Drug Name
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2360065
- UMLS CUI [1,2]
- C1276996
Descripción
Taking
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1290952
- UMLS CUI [1,2]
- C1276996
Descripción
Date dose taken
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [1,3]
- C1276996
Descripción
Time dose taken
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [1,3]
- C1276996
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Week 15 - Visit 13: 7-Day Follow-up
- StudyEvent: ODM
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