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ID

34747

Description

Study ID: 101998 Clinical Study ID: 101998 Study Title: A randomized, double-blind, parallel group, placebo-controlled, single-attack evaluation of the efficacy and tolerability of TREXIMA™ (sumatriptan 85mg/naproxen sodium 500mg)* tablets vs placebo when administered during the mild pain phase of a migraine Patient Level Data Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier Sponsor GlaxoSmithKline Collaborators N/A Phase Phase 3 Study Recruitment Status Completed Generic Name sumatriptan Trade Name Imitrex ,Imiject ,Imigran Study Indication Migraine Disorders The purpose of this form is to document the subjects study participation status. It should be filled out at the screening visit.

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Versions (3)
  1. 18/01/2019 18/01/2019 -
  2. 23/01/2019 23/01/2019 -
  3. 26/01/2019 26/01/2019 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

26 janvier 2019

DOI

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Licence

Creative Commons BY-NC 3.0
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    Efficacy and Tolerability of TREXIMA Tablets vs. Placebo During Mild Migraine Study ID 101998

    Anglais

    Study Participation Status

    1 Formulaires  
    Administrative Data
    Description

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Identifier
    Description

    Subject Identifier

    Type de données

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Visit Date
    Description

    Visit Date

    Type de données

    date

    Alias
    UMLS CUI [1]
    C1320303
    Randomisation Number
    Description

    Randomisation Number

    Alias
    UMLS CUI-1
    C0034656
    UMLS CUI-2
    C0237753
    Randomisation Number
    Description

    Record randomisation number.

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C0034656
    UMLS CUI [1,2]
    C0237753
    Investigational Product Container Number
    Description

    Investigational Product Container Number

    Alias
    UMLS CUI-1
    C0304229
    UMLS CUI-2
    C0180098
    UMLS CUI-3
    C0600091
    Investigational Product Container Number
    Description

    Record the identifying number from the investigational product container dispensed at this visit.

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C0304229
    UMLS CUI [1,2]
    C0180098
    UMLS CUI [1,3]
    C0600091
    Previous Clinical Trial Participation (Migraine Treatment)
    Description

    Previous Clinical Trial Participation (Migraine Treatment)

    Alias
    UMLS CUI-1
    C2348568
    UMLS CUI-2
    C0149931
    UMLS CUI-3
    C0087111
    Did the subject participate in any other research studies of migraine treatments in the past 3 years?
    Description

    Previous Clinical Trial Participation (Migraine Treatment)

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C2348568
    UMLS CUI [1,2]
    C0149931
    UMLS CUI [1,3]
    C0087111
    If Yes, record how many research studies.
    Description

    Number of Research Studies

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C2348568
    UMLS CUI [1,2]
    C1265611
    PRIOR PARTICIPATION IN SUMATRIPTAN 85MG / NAPROXEN SODIUM 500MG TABLET STUDIES
    Description

    PRIOR PARTICIPATION IN SUMATRIPTAN 85MG / NAPROXEN SODIUM 500MG TABLET STUDIES

    Alias
    UMLS CUI-1
    C2348568
    UMLS CUI-2
    C0075632
    UMLS CUI-3
    C0027396
    Did the subject participate in a previous study of sumatriptan 85mg/naproxen sodium 500mg tablets?
    Description

    Previous Study Participation of Sumatriptan/Naproxen

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C2348568
    UMLS CUI [1,2]
    C0075632
    UMLS CUI [1,3]
    C0027396
    Previous Administrative Data
    Description

    Previous Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    UMLS CUI-2
    C0205156
    Study Number
    Description

    Study Number

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C0600091
    Previous Protocol Number
    Description

    Previous Protocol Number

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C3274381
    UMLS CUI [1,2]
    C0205156
    Previous Centre Number
    Description

    Previous Centre Number

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C0600091
    UMLS CUI [1,2]
    C0019994
    UMLS CUI [1,3]
    C0205156
    Previous Subject Number
    Description

    Previous Subject Number

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C2348585
    UMLS CUI [1,2]
    C0205156
    Retour au début de la page

    Similar models

    Study Participation Status

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Subject Identifier
    Item
    Subject Identifier
    integer
    C2348585 (UMLS CUI [1])
    Visit Date
    Item
    Visit Date
    date
    C1320303 (UMLS CUI [1])
    Item Group
    Randomisation Number
    C0034656 (UMLS CUI-1)
    C0237753 (UMLS CUI-2)
    Randomisation Number
    Item
    Randomisation Number
    integer
    C0034656 (UMLS CUI [1,1])
    C0237753 (UMLS CUI [1,2])
    Item Group
    Investigational Product Container Number
    C0304229 (UMLS CUI-1)
    C0180098 (UMLS CUI-2)
    C0600091 (UMLS CUI-3)
    Investigational Product Container Number
    Item
    Investigational Product Container Number
    integer
    C0304229 (UMLS CUI [1,1])
    C0180098 (UMLS CUI [1,2])
    C0600091 (UMLS CUI [1,3])
    Item Group
    Previous Clinical Trial Participation (Migraine Treatment)
    C2348568 (UMLS CUI-1)
    C0149931 (UMLS CUI-2)
    C0087111 (UMLS CUI-3)
    Item
    Did the subject participate in any other research studies of migraine treatments in the past 3 years?
    text
    C2348568 (UMLS CUI [1,1])
    C0149931 (UMLS CUI [1,2])
    C0087111 (UMLS CUI [1,3])
    Previous Clinical Trial Participation (Migraine Treatment)
    Code List
    Did the subject participate in any other research studies of migraine treatments in the past 3 years?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Number of Research Studies
    Item
    If Yes, record how many research studies.
    integer
    C2348568 (UMLS CUI [1,1])
    C1265611 (UMLS CUI [1,2])
    Item Group
    PRIOR PARTICIPATION IN SUMATRIPTAN 85MG / NAPROXEN SODIUM 500MG TABLET STUDIES
    C2348568 (UMLS CUI-1)
    C0075632 (UMLS CUI-2)
    C0027396 (UMLS CUI-3)
    Item
    Did the subject participate in a previous study of sumatriptan 85mg/naproxen sodium 500mg tablets?
    text
    C2348568 (UMLS CUI [1,1])
    C0075632 (UMLS CUI [1,2])
    C0027396 (UMLS CUI [1,3])
    Previous Study Participation of Sumatriptan/Naproxen
    Code List
    Did the subject participate in a previous study of sumatriptan 85mg/naproxen sodium 500mg tablets?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Item Group
    Previous Administrative Data
    C1320722 (UMLS CUI-1)
    C0205156 (UMLS CUI-2)
    Item
    Study Number
    integer
    C0008976 (UMLS CUI [1,1])
    C0600091 (UMLS CUI [1,2])
    Study Number
    Code List
    Study Number
    CL Item
    1 (1)
    CL Item
    2 (2)
    CL Item
    3 (3)
    Item
    Previous Protocol Number
    text
    C3274381 (UMLS CUI [1,1])
    C0205156 (UMLS CUI [1,2])
    Previous Protocol Number
    Code List
    Previous Protocol Number
    CL Item
    MT400-104 (MT400-104)
    CL Item
    MT400-204 (MT400-204)
    CL Item
    MT400-301 (MT400-301)
    CL Item
    MT400-302 (MT400-302)
    CL Item
    MT400-303 (MT400-303)
    Previous Centre Number
    Item
    Previous Centre Number
    integer
    C0600091 (UMLS CUI [1,1])
    C0019994 (UMLS CUI [1,2])
    C0205156 (UMLS CUI [1,3])
    Previous Subject Number
    Item
    Previous Subject Number
    integer
    C2348585 (UMLS CUI [1,1])
    C0205156 (UMLS CUI [1,2])
    Retour au début de la page 

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