ID
29787
Description
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 10 - Visit 10.
Link
https://clinicaltrials.gov/ct2/show/NCT00086593
Keywords
Versions (1)
- 4/19/18 4/19/18 - Sarah Riepenhausen
Copyright Holder
GlaxoSmithKline
Uploaded on
April 19, 2018
DOI
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License
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 10 - Visit 10
- StudyEvent: ODM
Description
Psychiatric Evaluation
Alias
- UMLS CUI-1
- C0846574
Description
Positive and Negative Syndrome Scale (PANSS)
Data type
integer
Alias
- UMLS CUI [1]
- C0451383
Description
5 Subdomains: Affective Flattening or Blunting Alogia Avolition - Apathy Anhedonia - Asociality Attention
Data type
integer
Alias
- UMLS CUI [1,1]
- C4511599
- UMLS CUI [1,2]
- C0681889
- UMLS CUI [1,3]
- C0036341
Description
Calgary Depression Scale for Schizophrenia (CDSS)
Data type
integer
Alias
- UMLS CUI [1,1]
- C0679604
- UMLS CUI [1,2]
- C0036341
Description
Clinicians Global Impressions - Severity (CGI-S)
Data type
integer
Alias
- UMLS CUI [1]
- C3639887
Description
Clinicians Global Impressions - Improvement (CGI-I)
Data type
integer
Alias
- UMLS CUI [1]
- C3639888
Description
Brief Assessment of Cognition for Schizophrenia (BACS)
Data type
integer
Alias
- UMLS CUI [1]
- C4055347
Description
Pharmacokinetic Sampling
Description
Sample No.: BLD005
Data type
date
Alias
- UMLS CUI [1,1]
- C0178913
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0201734
Description
Sampling Time
Data type
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0005834
- UMLS CUI [1,3]
- C0201734
Description
Sample No.: BLD005
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0201734
Description
Atypical Antipsychotic Dosing
Alias
- UMLS CUI-1
- C0040615
- UMLS CUI-2
- C0205182
- UMLS CUI-3
- C0178602
Description
Drug Name
Data type
text
Alias
- UMLS CUI [1,1]
- C2360065
- UMLS CUI [1,2]
- C1276996
Description
Taking
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1290952
- UMLS CUI [1,2]
- C1276996
Description
Date dose taken
Data type
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [1,3]
- C1276996
Description
Time dose taken
Data type
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [1,3]
- C1276996
Description
Investigational Product Dosing
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0678766
Similar models
Week 10 - Visit 10
- StudyEvent: ODM
C0518766 (UMLS CUI [1,2])
C0681889 (UMLS CUI [1,2])
C0036341 (UMLS CUI [1,3])
C0036341 (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])
C0678766 (UMLS CUI-2)
C0013227 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
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