ID
29786
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 8 - Visit 9.
Lien
https://clinicaltrials.gov/ct2/show/NCT00086593
Mots-clés
Versions (1)
- 19/04/2018 19/04/2018 - Sarah Riepenhausen
Détendeur de droits
GlaxoSmithKline
Téléchargé le
19 avril 2018
DOI
Pour une demande vous connecter.
Licence
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 8 - Visit 9
- StudyEvent: ODM
Description
Psychiatric Evaluation
Alias
- UMLS CUI-1
- C0846574 (Psychiatric evaluation)
Description
Positive and Negative Syndrome Scale (PANSS)
Type de données
integer
Alias
- UMLS CUI [1]
- C0451383 (Positive and negative syndrome scale)
- SNOMED
- 273703003
Description
Clinicians Global Impressions - Severity (CGI-S)
Type de données
integer
Alias
- UMLS CUI [1]
- C3639887 (CGI - Severity of Illness)
Description
Clinicians Global Impressions - Improvement (CGI-I)
Type de données
integer
Alias
- UMLS CUI [1]
- C3639888 (CGI - Global Improvement)
Description
Simpson Angus Scale
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0681889 (rating scale)
- UMLS CUI [1,2]
- C0041755 (Adverse reaction to drug)
- SNOMED
- 62014003
- LOINC
- LA7429-9
- UMLS CUI [1,3]
- C0015371 (Extrapyramidal Disorders)
- SNOMED
- 76349003
Description
The Barnes Akathisia Scale
Type de données
integer
Alias
- UMLS CUI [1]
- C3541345 (Barnes Akathisia Rating Scale Questionnaire)
Description
Abnormal Involuntary Movement Scale (AIMS)
Type de données
integer
Alias
- UMLS CUI [1]
- C0450978 (Abnormal Involuntary Movement Scale)
- SNOMED
- 273256000
Description
Pharmacokinetic Sampling
Description
Sample No.: BLD004
Type de données
date
Alias
- UMLS CUI [1,1]
- C0178913 (Blood specimen)
- SNOMED
- 119297000
- UMLS CUI [1,2]
- C0011008 (Date in time)
- SNOMED
- 410671006
- UMLS CUI [1,3]
- C0201734 (Pharmacokinetic study)
- SNOMED
- 48684007
Description
Sampling Time
Type de données
time
Alias
- UMLS CUI [1,1]
- C0040223 (Time)
- SNOMED
- 410670007
- LOINC
- LP73517-2
- UMLS CUI [1,2]
- C0005834 (Collection of blood specimen for laboratory procedure)
- SNOMED
- 82078001
- LOINC
- LP125037-4
- UMLS CUI [1,3]
- C0201734 (Pharmacokinetic study)
- SNOMED
- 48684007
Description
Sample No.: BLD004
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0005834 (Collection of blood specimen for laboratory procedure)
- SNOMED
- 82078001
- LOINC
- LP125037-4
- UMLS CUI [1,2]
- C0201734 (Pharmacokinetic study)
- SNOMED
- 48684007
Description
Atypical Antipsychotic Dosing
Alias
- UMLS CUI-1
- C0040615 (Antipsychotic Agents)
- SNOMED
- 10784006
- LOINC
- LP18073-4
- UMLS CUI-2
- C0205182 (Atypical)
- SNOMED
- 112231000
- LOINC
- LA13702-8
- UMLS CUI-3
- C0178602 (Dosage)
- SNOMED
- 260911001
- LOINC
- LP7180-5
Description
Drug Name
Type de données
text
Alias
- UMLS CUI [1,1]
- C2360065 (Medication name)
- LOINC
- MTHU027854
- UMLS CUI [1,2]
- C1276996 (Atypical antipsychotic)
Description
Taking
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1290952 (Taking medication (activity))
- SNOMED
- 129019007
- UMLS CUI [1,2]
- C1276996 (Atypical antipsychotic)
Description
Date dose taken
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008 (Date in time)
- SNOMED
- 410671006
- UMLS CUI [1,2]
- C0178602 (Dosage)
- SNOMED
- 260911001
- LOINC
- LP7180-5
- UMLS CUI [1,3]
- C1276996 (Atypical antipsychotic)
Description
Time dose taken
Type de données
time
Alias
- UMLS CUI [1,1]
- C0040223 (Time)
- SNOMED
- 410670007
- LOINC
- LP73517-2
- UMLS CUI [1,2]
- C0178602 (Dosage)
- SNOMED
- 260911001
- LOINC
- LP7180-5
- UMLS CUI [1,3]
- C1276996 (Atypical antipsychotic)
Description
Investigational Product Dosing
Alias
- UMLS CUI-1
- C0304229 (Experimental drug)
- UMLS CUI-2
- C0678766 (Drug dose)
- SNOMED
- 398232005
Description
Planned relative Time: Day before Clinic Visit
Type de données
date
Alias
- UMLS CUI [1,1]
- C0011008 (Date in time)
- SNOMED
- 410671006
- UMLS CUI [1,2]
- C0013227 (Pharmaceutical Preparations)
- SNOMED
- 763158003
- LOINC
- LP100609-9
Description
Time dose taken
Type de données
time
Alias
- UMLS CUI [1,1]
- C0040223 (Time)
- SNOMED
- 410670007
- LOINC
- LP73517-2
- UMLS CUI [1,2]
- C0013227 (Pharmaceutical Preparations)
- SNOMED
- 763158003
- LOINC
- LP100609-9
Similar models
Week 8 - Visit 9
- StudyEvent: ODM
C0518766 (UMLS CUI [1,2])
C0041755 (UMLS CUI [1,2])
C0015371 (UMLS CUI [1,3])
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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