ID
29790
Beschrijving
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
Trefwoorden
Versies (1)
- 19-04-18 19-04-18 - Sarah Riepenhausen
Houder van rechten
GlaxoSmithKline
Geüploaded op
19 april 2018
DOI
Voor een aanvraag inloggen.
Licentie
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
Beschrijving
Pregnancy Test
Alias
- UMLS CUI-1
- C0430056
Beschrijving
Pregnancy Test applicable
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0032976
- UMLS CUI [1,2]
- C1706839
Beschrijving
Pregnancy test performed
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0032976
- UMLS CUI [1,2]
- C0884358
Beschrijving
If positive, complete PREGNANCY NOTIFICATION FORM.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0032976
- UMLS CUI [1,2]
- C1274040
Beschrijving
Pharmacokinetic Sampling
Beschrijving
Sample No.: BLD007
Datatype
date
Alias
- UMLS CUI [1,1]
- C0178913
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0201734
Beschrijving
Sampling Time
Datatype
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0005834
- UMLS CUI [1,3]
- C0201734
Beschrijving
Sample No.: BLD007
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0201734
Beschrijving
Atypical Antipsychotic Dosing
Alias
- UMLS CUI-1
- C0040615
- UMLS CUI-2
- C0205182
- UMLS CUI-3
- C0178602
Beschrijving
Drug Name
Datatype
text
Alias
- UMLS CUI [1,1]
- C2360065
- UMLS CUI [1,2]
- C1276996
Beschrijving
Taking
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1290952
- UMLS CUI [1,2]
- C1276996
Beschrijving
Date dose taken
Datatype
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [1,3]
- C1276996
Beschrijving
Time dose taken
Datatype
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [1,3]
- C1276996
Similar models
Week 15 - Visit 13: 7-Day Follow-up
- StudyEvent: ODM
C0518766 (UMLS CUI [1,2])
C1706839 (UMLS CUI [1,2])
C0884358 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0201734 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,2])
C0201734 (UMLS CUI [1,3])
C0201734 (UMLS CUI [1,2])
C0205182 (UMLS CUI-2)
C0178602 (UMLS CUI-3)
C1276996 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C1276996 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,2])
C1276996 (UMLS CUI [1,3])
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