ID

36274

Description

Study ID: 101963 Clinical Study ID: SCA101963 Study Title: A randomised, blinded, parallel group study to investigate the potential pharmacokinetic interaction between lamotrigine and risperidone in healthy, non-smoking, male volunteers. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: lamotrigine Trade Name: Lamictal XR,Lamictal,LAMICTIN Study Indication: Schizophrenia

Keywords

  1. 4/28/19 4/28/19 -
Copyright Holder

GlaxoSmithKline

Uploaded on

April 28, 2019

DOI

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License

Creative Commons BY-NC 3.0

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Potential Pharmacokinetic Interaction between Lamotrigine and Risperidone; 101963

Sessions

  1. StudyEvent: ODM
    1. Sessions
SESSION 2
Description

SESSION 2

Alias
UMLS CUI-1
C0008976
UMLS CUI-2
C1883016
Target Dosing Time
Description

Clinical Trials, Session, Dosage, Time

Data type

time

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C1883017
UMLS CUI [1,3]
C0178602
UMLS CUI [1,4]
C0040223
Day
Description

Clinical Trials, Session, Day, Numbers

Data type

text

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C1883017
UMLS CUI [1,3]
C0439228
UMLS CUI [1,4]
C0237753
Date
Description

Clinical Trials, Session, Date in time

Data type

date

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C1883017
UMLS CUI [1,3]
C0011008
Time
Description

Clinical Trials, Session, Time

Data type

time

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C1883017
UMLS CUI [1,3]
C0040223
Initial
Description

Clinical Trials, Session, Person Initials

Data type

text

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C1883017
UMLS CUI [1,3]
C2986440

Similar models

Sessions

  1. StudyEvent: ODM
    1. Sessions
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
SESSION 2
C0008976 (UMLS CUI-1)
C1883016 (UMLS CUI-2)
Clinical Trials, Session, Dosage, Time
Item
Target Dosing Time
time
C0008976 (UMLS CUI [1,1])
C1883017 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
Item
Day
text
C0008976 (UMLS CUI [1,1])
C1883017 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,3])
C0237753 (UMLS CUI [1,4])
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75 PM (87)
Clinical Trials, Session, Date in time
Item
Date
date
C0008976 (UMLS CUI [1,1])
C1883017 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Clinical Trials, Session, Time
Item
Time
time
C0008976 (UMLS CUI [1,1])
C1883017 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Clinical Trials, Session, Person Initials
Item
Initial
text
C0008976 (UMLS CUI [1,1])
C1883017 (UMLS CUI [1,2])
C2986440 (UMLS CUI [1,3])

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