0 Évaluations
ID

26109

Description

Study ID: 101468/219 Clinical Study ID: 101468/219 Study Title:An open label, randomised, five-way crossover single-dose pharmacokinetic study to assess dosage strength equivalence of ropinirole CR in healthy male and female 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: ropinirole Trade Name: Requip Study Indication : Parkinson Disease Documentation part: Concomitant Medication

Mots-clés

Versions (1)
  1. 09/10/2017 09/10/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

9 octobre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Retour au modèle Commentaires
Groupe Item commentaires pour :

Item commentaires pour :

  • Plus récent
  • Plus ancien
  • Favori
  • Plus récent
    • Plus récent
    • Plus ancien
    • Favori

    Aucun commentaire

    Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

    Dose strength equivalence of ropinirole CR in healthy adults Concomitant Medication 101468/219

    Anglais

    Concomitant Medication Dose strength equivalence of ropinirole CR in healthy adults 101468/219

    1 Formulaires  
    Concomitant Medication
    Description

    Concomitant Medication

    Alias
    UMLS CUI-1
    C2347852
    UMLS CUI-2
    C0244821
    Are there any concomitant medication CHANGES since the start of the study?
    Description

    If ’YES’, please record all medications used below. Where appropriate, medical conditions should be recorded on the Adverse Events Form, utilizing the same terminology. If a medication has had a dosage change it must be recorded with the start and stop date.

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2347852
    drug name
    Description

    Trade Name Preferred

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C2360065
    UMLS CUI [1,2]
    C2347852
    Single Dose/Unit
    Description

    dose per unit

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C3174092
    UMLS CUI [1,2]
    C2347852
    Frequency of this Dose
    Description

    medication frequency

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C3476109
    UMLS CUI [1,2]
    C2347852
    Route
    Description

    drug application route

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0013153
    UMLS CUI [1,2]
    C2347852
    Indication
    Description

    medication indication

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C3146298
    UMLS CUI [1,2]
    C2347852
    Duration
    Description

    duration of medication

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0449238
    UMLS CUI [1,2]
    C2347852
    End Date
    Description

    end date of medication

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0806020
    Continuing at end of study?
    Description

    continuing medication

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2826666
    Retour au début de la page

    Similar models

    Concomitant Medication Dose strength equivalence of ropinirole CR in healthy adults 101468/219

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Concomitant Medication
    C2347852 (UMLS CUI-1)
    C0244821 (UMLS CUI-2)
    concomitant medication
    Item
    Are there any concomitant medication CHANGES since the start of the study?
    boolean
    C2347852 (UMLS CUI [1])
    drug name
    Item
    drug name
    text
    C2360065 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    dose per unit
    Item
    Single Dose/Unit
    integer
    C3174092 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    medication frequency
    Item
    Frequency of this Dose
    text
    C3476109 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    drug application route
    Item
    Route
    text
    C0013153 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    medication indication
    Item
    Indication
    text
    C3146298 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    duration of medication
    Item
    Duration
    text
    C0449238 (UMLS CUI [1,1])
    C2347852 (UMLS CUI [1,2])
    end date of medication
    Item
    End Date
    date
    C2347852 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    continuing medication
    Item
    Continuing at end of study?
    boolean
    C2826666 (UMLS CUI [1])
    Retour au début de la page 

    Aide

    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