ID

33653

Descripción

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 is for documentation of the dermatological examination. It should be filled out at each treatment period and follow-up visit. Note: In the event of a subject experiencing a suspected drug induced rash, the subject should be withdrawn from the study immediately. 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

Palabras clave

Versiones (2)
  1. 3/12/18 3/12/18 -
  2. 18/12/18 18/12/18 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

18 de diciembre de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

  • El más nuevo
  • Más antiguo
  • Popular
  • El más nuevo
    • El más nuevo
    • Más antiguo
    • Popular

    Sin comentarios

    Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

    Effect of Lamictal on Resting Motor Threshold Study-ID 107434

    Inglés

    Dermatological Examination Form

    1 formularios  
    Administrative Data
    Descripción

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Screening number
    Descripción

    Subject Screening No.

    Tipo de datos

    integer

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

    Subject Number

    Tipo de datos

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Study Visit
    Descripción

    Study Visit

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0545082
    Dermatological Examination
    Descripción

    Dermatological Examination

    Alias
    UMLS CUI-1
    C0560169
    Protocol Time
    Descripción

    Protocol Time

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0040223
    UMLS CUI [1,2]
    C2348563
    Study Day
    Descripción

    Study Day

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C2826182
    Date of Assessment
    Descripción

    Date of Assessment

    Tipo de datos

    date

    Alias
    UMLS CUI [1]
    C2985720
    Actual Time
    Descripción

    Actual Time

    Tipo de datos

    time

    Alias
    UMLS CUI [1]
    C0040223
    Has a Dermatological examination been performed?
    Descripción

    If no, please comment If yes, The following need to be completed: - Add a comment on the “Additional Information” page of the CRF - Complete the Adverse Event source document. - Complete the Dermatological / Hypersensitivity Adverse Event page

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0560169
    Comment
    Descripción

    Comment

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0947611
    Has the subject experienced any type of rash?
    Descripción

    If yes, complete the subject’s Adverse Event source document book.

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0015230
    How long after administration of the drug did the rash occur?
    Descripción

    Time After Administration Exanthema Occurred

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0015230
    UMLS CUI [1,2]
    C0040223
    UMLS CUI [1,3]
    C0439568
    In the opinion of the physician, is the subject experiencing a suspected drug induced rash?
    Descripción

    If yes, complete the “Record of Rash” page at the back of the CRF.

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0015230
    UMLS CUI [1,2]
    C0458082
    Was a dermatologist consulted?
    Descripción

    Dermatologist Consulted

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0259831
    UMLS CUI [1,2]
    C0009818
    Physician's Signature
    Descripción

    Physician's Signature

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C1519316
    UMLS CUI [1,2]
    C0031831
    Volver a la parte superior de la página

    Similar models

    Dermatological Examination Form

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    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
    Study Visit
    text
    C0545082 (UMLS CUI [1])
    Study Visit
    Code List
    Study Visit
    CL Item
    Treatment Period 1 (Treatment Period 1)
    CL Item
    Treatment Period 2 (Treatment Period 2)
    CL Item
    Treatment Period 3 (Treatment Period 3)
    CL Item
    Follow-Up Visit (Follow-Up Visit)
    Item Group
    Dermatological Examination
    C0560169 (UMLS CUI-1)
    Item
    Protocol Time
    text
    C0040223 (UMLS CUI [1,1])
    C2348563 (UMLS CUI [1,2])
    Protocol Time
    Code List
    Protocol Time
    CL Item
    Pre Dose (Pre Dose)
    CL Item
    48h00 post dose (48h00 post dose)
    CL Item
    24h00 post dose (24h00 post dose)
    CL Item
    216h00 post dose (216h00 post dose)
    Item
    Study Day
    text
    C2826182 (UMLS CUI [1])
    Study Day
    Code List
    Study Day
    CL Item
    Day 1 (Day 1)
    CL Item
    Day 3 (Day 3)
    CL Item
    Day 2 (Day 2)
    CL Item
    Day 10 (Day 10)
    Date of Assessment
    Item
    Date of Assessment
    date
    C2985720 (UMLS CUI [1])
    Actual Time
    Item
    Actual Time
    time
    C0040223 (UMLS CUI [1])
    Dermatological Examination Performed
    Item
    Has a Dermatological examination been performed?
    boolean
    C0560169 (UMLS CUI [1])
    Comment
    Item
    Comment
    text
    C0947611 (UMLS CUI [1])
    Rashes
    Item
    Has the subject experienced any type of rash?
    boolean
    C0015230 (UMLS CUI [1])
    Time After Administration Exanthema Occurred
    Item
    How long after administration of the drug did the rash occur?
    text
    C0015230 (UMLS CUI [1,1])
    C0040223 (UMLS CUI [1,2])
    C0439568 (UMLS CUI [1,3])
    Sespected Drug induced Rash
    Item
    In the opinion of the physician, is the subject experiencing a suspected drug induced rash?
    boolean
    C0015230 (UMLS CUI [1,1])
    C0458082 (UMLS CUI [1,2])
    Dermatologist Consulted
    Item
    Was a dermatologist consulted?
    boolean
    C0259831 (UMLS CUI [1,1])
    C0009818 (UMLS CUI [1,2])
    Physician's Signature
    Item
    Physician's Signature
    text
    C1519316 (UMLS CUI [1,1])
    C0031831 (UMLS CUI [1,2])
    Volver a la parte superior de la página 

    Ayuda

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial