ID
37679
Descripción
Study ID: 105377 Clinical Study ID: 105377 Study Title: A randomised, open-label, parallel-group design study to evaluate the pharmacokinetic characteristics, safety and tolerability of single oral doses of three prototype 300mg enteric coated - modified release formulations of Lamotrigine in healthy subjects. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Lamotrigine Study Indication: Epilepsy
Palabras clave
Versiones (1)
- 16/8/19 16/8/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
16 de agosto de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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Pharmacokinetic characteristics, safety and tolerability of single oral doses of three prototype 300mg enteric coated - modified release formulations of Lamotrigine (Study ID: 105377)
Logs/ Repeats - Logs and Repeats; Adverse Events
- StudyEvent: ODM
Descripción
Logs and Repeats - Adverse event/ Concomitant Medication/ Repeat Assessment Check Questions
Alias
- UMLS CUI-1
- C1708728
- UMLS CUI-2
- C0205341
- UMLS CUI-3
- C0877248
- UMLS CUI-4
- C1516048
- UMLS CUI-5
- C2347852
- UMLS CUI-6
- C1516048
Descripción
Were any concomitant medications taken by the subject during the study?
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2347852
Descripción
Did the subject experience any adverse events during the study?
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0877248
Descripción
Were any repeat haematology or clinical chemistry samples taken?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0018941
- UMLS CUI [1,2]
- C0200345
Descripción
Were any repeat urinalysis samples taken?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C0205341
Descripción
Were any repeat vital signs recorded?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0205341
Descripción
Were any repeat vital signs recorded?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0205341
Descripción
Were any repeat PK samples taken?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1277698
- UMLS CUI [1,2]
- C0031327
- UMLS CUI [1,3]
- C0205341
Descripción
Adverse Event (AE)
Alias
- UMLS CUI-1
- C0877248
Descripción
Adverse Event - Sequence Number
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C2348184
Descripción
Diagnosis Only (if known) Otherwise Sign/Symptom
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0877248
Descripción
Adverse Event - Modified term
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0877248
Descripción
Adverse Event - MedDRA synonym
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C1140263
Descripción
Adverse Event - MedDRA lower level term code
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C3898442
Descripción
Adverse Event - Failed coding
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0805701
- UMLS CUI [1,3]
- C0231175
Descripción
Adverse Event Start Date and Time
Tipo de datos
datetime
Alias
- UMLS CUI [1]
- C2826806
Descripción
Adverse Event Outcome
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1705586
Descripción
Adverse Event End Date and Time
Tipo de datos
datetime
Alias
- UMLS CUI [1]
- C2826793
Descripción
Adverse Event - Date and Time of Death
Tipo de datos
datetime
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C1148348
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C1301931
Descripción
Adverse Event Frequency
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0439603
Descripción
Adverse Event Maximum Intensity
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C0518690
Descripción
Action Taken with Investigational Product(s) as a Result of the AE
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C1518404
Descripción
Did the subject withdraw from study as a result of this AE?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1710677
- UMLS CUI [1,2]
- C1518404
Descripción
Is there a reasonable possibility that the AE may have been caused by the investigational product?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0439849
Descripción
If Yes, complete paper SAE form and fax to GSK Safety within 24 hr
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1519255
Descripción
Check all that apply
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1705586
- UMLS CUI [1,2]
- C1519255
Descripción
If other Serious Adverse Event Outcome, specify
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1705586
- UMLS CUI [1,2]
- C1519255
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Descripción
Was this SAE caused by an activity related to study participation (e.g., procedures)?
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C3641099
Similar models
Logs/ Repeats - Logs and Repeats; Adverse Events
- StudyEvent: ODM
C2985720 (UMLS CUI [1,2])
C0205341 (UMLS CUI-2)
C0877248 (UMLS CUI-3)
C1516048 (UMLS CUI-4)
C2347852 (UMLS CUI-5)
C1516048 (UMLS CUI-6)
C0200345 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,2])
C0205341 (UMLS CUI [1,3])
C0205341 (UMLS CUI [1,2])
C0205341 (UMLS CUI [1,2])
C0031327 (UMLS CUI [1,2])
C0205341 (UMLS CUI [1,3])
C2348184 (UMLS CUI [1,2])
C1140263 (UMLS CUI [1,2])
C3898442 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C1148348 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C1301931 (UMLS CUI [2,2])
C0439603 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C1518404 (UMLS CUI [1,2])
C1518404 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C3641099 (UMLS CUI [1,2])