0 Évaluations
ID

40732

Description

Study ID: 101468/218 Clinical Study ID: SKF-101468/218 Study Title:A Single-Blind, Randomised, Placebo-Controlled, Parallel-Group, Multicentre, Phase IIa Study to Determine the Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Restless Legs Syndrome

Mots-clés

Versions (1)
  1. 05/05/2020 05/05/2020 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

5 mai 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 4.0
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.

    Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/218

    Anglais

    Pregnancy Test

    1 Formulaires  
    1. StudyEvent: ODM
      1. Pregnancy Test
    Administrative
    Description

    Administrative

    Alias
    UMLS CUI-1
    C1320722 (Administrative documentation)
    SNOMED
    405624007
    Patient Number
    Description

    Patient Number

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Centre Number
    Description

    Centre Number

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0600091 (Identifier)
    SNOMED
    118522005
    LOINC
    LP31795-5
    UMLS CUI [1,2]
    C0019994 (Hospitals)
    Visit Date
    Description

    Visit Date

    Type de données

    date

    Alias
    UMLS CUI [1]
    C1320303 (Date of visit)
    SNOMED
    406543005
    Pregnancy Test
    Description

    Pregnancy Test

    Alias
    UMLS CUI-1
    C0032976 (Pregnancy Tests)
    SNOMED
    74036000
    Was a pregnancy test carried out?
    Description

    Was a pregnancy test carried out?

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0032976 (Pregnancy Tests)
    SNOMED
    74036000
    If no pregnancy test was carried out, specify reason
    Description

    If no pregnancy test was carried out, specify reason

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0032976 (Pregnancy Tests)
    SNOMED
    74036000
    UMLS CUI [1,2]
    C2826287 (Not-Done Reason)
    Date of pregnancy test
    Description

    Date of pregnancy test

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0032976 (Pregnancy Tests)
    SNOMED
    74036000
    UMLS CUI [1,2]
    C0011008 (Date in time)
    SNOMED
    410671006
    Result of Pregnancy Test
    Description

    Result of Pregnancy Test

    Type de données

    integer

    Alias
    UMLS CUI [1]
    C0427777 (Pregnancy test finding)
    SNOMED
    250421003
    Retour au début de la page

    Similar models

    Pregnancy Test

    1 Formulaires
    1. StudyEvent: ODM
      1. Pregnancy Test
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Administrative
    C1320722 (UMLS CUI-1)
    Patient Number
    Item
    Patient Number
    text
    C2348585 (UMLS CUI [1])
    Centre Number
    Item
    Centre Number
    text
    C0600091 (UMLS CUI [1,1])
    C0019994 (UMLS CUI [1,2])
    Visit Date
    Item
    Visit Date
    date
    C1320303 (UMLS CUI [1])
    Item Group
    Pregnancy Test
    C0032976 (UMLS CUI-1)
    Was a pregnancy test carried out?
    Item
    Was a pregnancy test carried out?
    boolean
    C0032976 (UMLS CUI [1])
    If no pregnancy test was carried out, specify reason
    Item
    If no pregnancy test was carried out, specify reason
    text
    C0032976 (UMLS CUI [1,1])
    C2826287 (UMLS CUI [1,2])
    Date of pregnancy test
    Item
    Date of pregnancy test
    date
    C0032976 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    Item
    Result of Pregnancy Test
    integer
    C0427777 (UMLS CUI [1])
    Result of Pregnancy Test
    Code List
    Result of Pregnancy Test
    CL Item
    Positive (1)
    CL Item
    Negative (2)
    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