ID
36206
Beschreibung
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
Stichworte
Versionen (1)
- 22.04.19 22.04.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
22. April 2019
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Potential Pharmacokinetic Interaction between Lamotrigine and Risperidone; 101963
Period 2 Days 74-75
- StudyEvent: ODM
Beschreibung
Drug Screen
Alias
- UMLS CUI-1
- C0373483
Beschreibung
Drug screen, Sampling, Date in time, Time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C0373483
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Beschreibung
Drug screen, Cocaine
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0373483
- UMLS CUI [1,2]
- C0009170
Beschreibung
Drug screen, Amphetamines
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0373483
- UMLS CUI [1,2]
- C0002667
Beschreibung
Drug screen, Benzodiazepines
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0373483
- UMLS CUI [1,2]
- C0005064
Beschreibung
Drug screen, Cannabinoids
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0373483
- UMLS CUI [1,2]
- C0006864
Beschreibung
Drug screen, Opiates
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0373483
- UMLS CUI [1,2]
- C0376196
Beschreibung
Drug screen, Barbiturates
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0373483
- UMLS CUI [1,2]
- C0004745
Beschreibung
Alcohol Breath Test
Alias
- UMLS CUI-1
- C0202306
Beschreibung
Pregnancy
Alias
- UMLS CUI-1
- C0032961
Beschreibung
Electronically transferred laboratory data - Clinical Chemistry, Haematology
Alias
- UMLS CUI-1
- C0008000
- UMLS CUI-2
- C0018941
Beschreibung
Chemistry, Clinical, Hematologic tests, Relative time, Planned
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0018941
- UMLS CUI [1,3]
- C0439564
- UMLS CUI [1,4]
- C1301732
Beschreibung
Chemistry, Clinical, Hematologic tests, Sampling, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0018941
- UMLS CUI [1,3]
- C0870078
- UMLS CUI [1,4]
- C0011008
Beschreibung
Chemistry, Clinical, Hematologic tests, Sampling, Time
Datentyp
time
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0018941
- UMLS CUI [1,3]
- C0870078
- UMLS CUI [1,4]
- C0040223
Beschreibung
Investigational Product
Alias
- UMLS CUI-1
- C0304229
Beschreibung
Experimental drug, Relative time, Planned
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0439564
- UMLS CUI [1,3]
- C1301732
Beschreibung
Experimental drug, Dosage, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [1,3]
- C0011008
Beschreibung
Experimental drug, Dosage, Time
Datentyp
time
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0178602
- UMLS CUI [1,3]
- C0040223
Ähnliche Modelle
Period 2 Days 74-75
- StudyEvent: ODM
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0002667 (UMLS CUI [1,2])
C0005064 (UMLS CUI [1,2])
C0006864 (UMLS CUI [1,2])
C0004745 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,2])
C0018941 (UMLS CUI-2)
C0018941 (UMLS CUI [1,2])
C0439564 (UMLS CUI [1,3])
C1301732 (UMLS CUI [1,4])
C0018941 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0018941 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0439564 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])