ID
29776
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 Screen Part 4: Psychiatric History and Evaluation, Medication.
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
Screen Part 4: Psychiatric History and Examination, Medication
- StudyEvent: ODM
Beschrijving
Prior Psychotropic Medication History
Alias
- UMLS CUI-1
- C0033978
- UMLS CUI-2
- C2826257
Beschrijving
Record over-the-counter and prescription drugs prescribed for CNS or psychiatric disorders.
Datatype
text
Alias
- UMLS CUI [1]
- C2360065
Beschrijving
Psychotropic Medication Dose
Datatype
float
Alias
- UMLS CUI [1,1]
- C3174092
- UMLS CUI [1,2]
- C0033978
Beschrijving
Units
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519795
- UMLS CUI [1,2]
- C3174092
- UMLS CUI [1,3]
- C0033978
Beschrijving
Frequency
Datatype
text
Alias
- UMLS CUI [1,1]
- C3476109
- UMLS CUI [1,2]
- C0033978
Beschrijving
Route
Datatype
text
Alias
- UMLS CUI [1,1]
- C0013153
- UMLS CUI [1,2]
- C0033978
Beschrijving
Date started
Datatype
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0033978
Beschrijving
If ongoing at baseline, record stop date as baseline visit date.
Datatype
date
Alias
- UMLS CUI [1,1]
- C0806020
- UMLS CUI [1,2]
- C0033978
Beschrijving
Conditions Treated / Indication
Datatype
text
Alias
- UMLS CUI [1,1]
- C3146298
- UMLS CUI [1,2]
- C0033978
Beschrijving
Tolerance
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0556444
- UMLS CUI [1,2]
- C0033978
Beschrijving
Response
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0521982
- UMLS CUI [1,2]
- C0033978
Beschrijving
Prior Non-psychotropic Medications
Alias
- UMLS CUI-1
- C2826257
Beschrijving
Record all prior non-psychotropic medications (if ongoing at Baseline, record Stop Date as Baseline Visit Date, record medication on Concomitant Medication page with Start Date as Baseline Visit Date and check Started Pre-Study). Trade names are preferred for all medications; this is particularly encouraged for all combination medications, e.g., multivitamins and cold medications. The subject should be encouraged to disclose all medications he/she has taken, including non-prescribed medications, herbal remedies, and nutritional supplements. Record nonpsychotropic medications taken within the last month. Record over-the-counter and prescription drugs prescribed, excluding those for CNS or psychiatric disorders.
Datatype
text
Alias
- UMLS CUI [1]
- C2360065
Beschrijving
Dose
Datatype
float
Alias
- UMLS CUI [1]
- C3174092
Beschrijving
Units
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519795
- UMLS CUI [1,2]
- C3174092
Beschrijving
Frequency
Datatype
text
Alias
- UMLS CUI [1]
- C3476109
Beschrijving
Route
Datatype
text
Alias
- UMLS CUI [1]
- C0013153
Beschrijving
Date started
Datatype
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0013227
Beschrijving
All ongoing medications should be recorded on the CONCOMITANT MEDICATION page after the Baseline Visit. Use Date of the Baseline Visit as Date Stopped for this page.
Datatype
date
Alias
- UMLS CUI [1]
- C0806020
Beschrijving
Conditions treated /Indication
Datatype
text
Alias
- UMLS CUI [1,1]
- C3146298
- UMLS CUI [1,2]
- C0013227
Beschrijving
Psychiatric Evaluation
Alias
- UMLS CUI-1
- C0846574
Beschrijving
Abnormal Involuntary Movement Scale
Datatype
integer
Alias
- UMLS CUI [1]
- C0450978
Beschrijving
Simpson Angus Scale
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0681889
- UMLS CUI [1,2]
- C0041755
- UMLS CUI [1,3]
- C0015371
Beschrijving
Barnes Akathisia Scale
Datatype
integer
Alias
- UMLS CUI [1]
- C3541345
Beschrijving
Positive and Negative Syndrome Scale
Datatype
integer
Alias
- UMLS CUI [1]
- C0451383
Beschrijving
Clinicians Global Impressions - Severity
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C3639708
- UMLS CUI [1,2]
- C3639887
Beschrijving
Pharmacokinetic Sampling
Alias
- UMLS CUI-1
- C0201734
- UMLS CUI-2
- C0005834
Beschrijving
Screening Sample number: BLD001
Datatype
date
Alias
- UMLS CUI [1,1]
- C0178913
- UMLS CUI [1,2]
- C0011008
Beschrijving
Time of Sampling
Datatype
time
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0040223
Beschrijving
Sample Number at Screening: BLD001
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0031328
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
Intake of antipsychotic drug
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0040615
- UMLS CUI [1,2]
- C1512806
Beschrijving
Date dose taken
Datatype
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C1276996
Beschrijving
Time
Datatype
time
Alias
- UMLS CUI [1,1]
- C0040223
- UMLS CUI [1,2]
- C1276996
Similar models
Screen Part 4: Psychiatric History and Examination, Medication
- StudyEvent: ODM
C1517194 (UMLS CUI [1,2])
C0220952 (UMLS CUI [1,2])
C0871189 (UMLS CUI [1,2])
C0748061 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
C2826257 (UMLS CUI-2)
C0033978 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,2])
C0033978 (UMLS CUI [1,3])
C0033978 (UMLS CUI [1,2])
C0033978 (UMLS CUI [1,2])
C0033978 (UMLS CUI [1,2])
C0033978 (UMLS CUI [1,2])
C0033978 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C0041755 (UMLS CUI [1,2])
C0015371 (UMLS CUI [1,3])
C3639887 (UMLS CUI [1,2])
C0005834 (UMLS CUI-2)
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0031328 (UMLS CUI [1,2])
C0205182 (UMLS CUI-2)
C0178602 (UMLS CUI-3)
C1512806 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C1276996 (UMLS CUI [1,3])
C1276996 (UMLS CUI [1,2])
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