ID

33690

Beskrivning

Study ID: 107434 Clinical Study ID: NAP107434 Study Title: A randomised, double-blind, double-dummy, placebo controlled, three-way cross-over study to investigate the effect of single oral doses of 100 mg GW273225 (4030W92) and 325 mg LAMICTAL on resting motor threshold in healthy subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Study Link: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GW273225 Trade Name: lamictal Study Indication: Bipolar Disorder This form contains information on adverse events that ocurred during the study. It should be filled out at the follow up visit. It should be filled out at the follow-up visit. Screening Visit: 28 days prior to first dosing. Treatment Period: The day before dosing, until 48h after dosing. Follow-Up: 14-21 days after last dose

Nyckelord

Versioner (3)
  1. 2018-12-03 2018-12-03 -
  2. 2018-12-19 2018-12-19 -
  3. 2019-01-11 2019-01-11 - Sarah Riepenhausen
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

19 december 2018

DOI

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Licens

Creative Commons BY-NC 3.0
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Effect of Lamictal on Resting Motor Threshold Study-ID 107434

Engelsk

AE Follow-Up

1 Formulär  
  1. StudyEvent: ODM
    1. AE Follow-Up
Administrative Data
Beskrivning

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Screening number
Beskrivning

Subject Screening No.

Datatyp

integer

Alias
UMLS CUI [1,1]
C0220908
UMLS CUI [1,2]
C0600091
Subject no.
Beskrivning

Subject Number

Datatyp

integer

Alias
UMLS CUI [1]
C2348585
AE Follow-Up
Beskrivning

AE Follow-Up

Alias
UMLS CUI-1
C1522577
UMLS CUI-2
C0877248
Has the subject’s adverse events been reviewed?
Beskrivning

Adverse Events Reviewed

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C1709940
Does the subject have any ongoing adverse event at follow up?
Beskrivning

If yes, update adverse event source document and provide adverse event follow up letter

Datatyp

boolean

Alias
UMLS CUI [1]
C2826663
AE letter given to subject?
Beskrivning

If no, provide reason If yes, provide date

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C1096774
UMLS CUI [1,3]
C1999230
Reason Letter Not Provided
Beskrivning

Reason Letter Not Provided

Datatyp

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C1096774
UMLS CUI [1,3]
C1999230
UMLS CUI [1,4]
C0392360
UMLS CUI [1,5]
C1272696
Date Letter Provided
Beskrivning

Date Letter Provided

Datatyp

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1096774
UMLS CUI [1,3]
C1999230
Conclusion
Beskrivning

Conclusion

Alias
UMLS CUI-1
C1707478
Clinical Staff initials
Beskrivning

Clinical Staff initials

Datatyp

text

Alias
UMLS CUI [1,1]
C2986440
UMLS CUI [1,2]
C0871685
Date
Beskrivning

Date

Datatyp

date

Alias
UMLS CUI [1]
C0011008
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Similar models

AE Follow-Up

1 Formulär
  1. StudyEvent: ODM
    1. AE Follow-Up
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Subject Screening No.
Item
Subject Screening number
integer
C0220908 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Subject Number
Item
Subject no.
integer
C2348585 (UMLS CUI [1])
Item Group
AE Follow-Up
C1522577 (UMLS CUI-1)
C0877248 (UMLS CUI-2)
Adverse Events Reviewed
Item
Has the subject’s adverse events been reviewed?
boolean
C0877248 (UMLS CUI [1,1])
C1709940 (UMLS CUI [1,2])
Adverse Event Ongoing
Item
Does the subject have any ongoing adverse event at follow up?
boolean
C2826663 (UMLS CUI [1])
AE letter Given to Subject
Item
AE letter given to subject?
boolean
C0877248 (UMLS CUI [1,1])
C1096774 (UMLS CUI [1,2])
C1999230 (UMLS CUI [1,3])
Reason Letter Not Provided
Item
Reason Letter Not Provided
text
C0877248 (UMLS CUI [1,1])
C1096774 (UMLS CUI [1,2])
C1999230 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,4])
C1272696 (UMLS CUI [1,5])
Date Letter Provided
Item
Date Letter Provided
date
C0011008 (UMLS CUI [1,1])
C1096774 (UMLS CUI [1,2])
C1999230 (UMLS CUI [1,3])
Item Group
Conclusion
C1707478 (UMLS CUI-1)
Clinical Staff initials
Item
Clinical Staff initials
text
C2986440 (UMLS CUI [1,1])
C0871685 (UMLS CUI [1,2])
Date
Item
Date
date
C0011008 (UMLS CUI [1])
Tillbaka till toppen 

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