0 Évaluations
ID

36916

Description

Study ID: 101468/201 Clinical Study ID: 101468/201 Study Title: A Single Blind, Parallel Group, Up-titration, Phase 1 Study in Healthy Volunteers to Determine a Starting Dose and Select an Up-titration Regimen for a new Formulation of Ropinirole 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: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication : Restless Legs Syndrome The Study consists of 21 Visits(Days): Screening (at least 21 days before dosing) Week 1: including Day 1-7 Week 2: including Day 8-14 Week 3: including Day 15-19 Follow-up Visit (7-14 days after last dose) This document contains the Baseline Signs And Symptoms for Screening form.

Mots-clés

Versions (1)
  1. 21/06/2019 21/06/2019 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

21 juin 2019

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.

    Determination of starting dose and up-titration regimen for a new formulation of Ropinirole in healthy adults, 101468/201

    Anglais

    Baseline Signs And Symptoms for Screening

    1 Formulaires  
    Administrative Data
    Description

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Volunteer panel number
    Description

    identification number

    Type de données

    integer

    Alias
    UMLS CUI [1]
    C1300638
    Subject number
    Description

    Subject number

    Type de données

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Non-serious Adverse Event
    Description

    Non-serious Adverse Event

    Alias
    UMLS CUI-1
    C1518404
    Were baseline events experienced during the module?
    Description

    Non-serious Adverse Event

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1518404
    Baseline sign/symptom
    Description

    Record any baseline events (using standard medical terminology) observed or elicited by the following direct question to the subject: “How do you feel?“ Provide the diagnosis, NOT symptoms where possible. (One baseline event per column)

    Type de données

    text

    Alias
    UMLS CUI [1]
    C0037088
    Onset Date
    Description

    day month year

    Type de données

    date

    Alias
    UMLS CUI [1]
    C2985916
    Onset Time
    Description

    00:00-23:59

    Type de données

    time

    Alias
    UMLS CUI [1,1]
    C0449244
    UMLS CUI [1,2]
    C1518404
    End Date
    Description

    day month year

    Type de données

    date

    Alias
    UMLS CUI [1]
    C2697886
    End Time
    Description

    00:00-23:59

    Type de données

    time

    Alias
    UMLS CUI [1,1]
    C1518404
    UMLS CUI [1,2]
    C1522314
    Outcome
    Description

    Outcome

    Type de données

    integer

    Alias
    UMLS CUI [1]
    C1705586
    Event course
    Description

    Experience Course

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C0877248
    UMLS CUI [1,2]
    C0750729
    No. of episodes
    Description

    Number of episodes

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C0877248
    UMLS CUI [1,2]
    C4086638
    Intensity (maximum)
    Description

    MILD: An event which is easily tolerated MODERATE: An event which is sufficiently discomforting to interfere with daily activity SEVERE: An event which prevents normal everyday activities

    Type de données

    integer

    Alias
    UMLS CUI [1]
    C1710066
    Relationship to study procedures performed prior to randomisation
    Description

    NOT RELATED: The event is definitely not related to the study procedures UNLIKELY: There are other more likely causes and the study procedures are not suspected as a cause SUSPECTED (REASONABLE POSSIBILITY): A direct cause and effect relationship between the study procedures and the event has not been demonstrated but there is a reasonable possibility that the study procedures were involved PROBABLE: There probably is a direct cause and effect relationship between the event and the study procedures

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C2700391
    Corrective Therapy
    Description

    If ‘Yes’, record details in the Concomitant Medication section and/or Healthcare Resource Utilisation form if appropriate

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0877248
    UMLS CUI [1,2]
    C0087111
    Was patient withdrawn due to this specific AE?
    Description

    patient withdrawn due to this specific AE

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0422727
    UMLS CUI [1,2]
    C1518404
    Investigator signature:
    Description

    Investigator signature

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2346576
    Date:
    Description

    day month year

    Type de données

    date

    Alias
    UMLS CUI [1]
    C0011008
    Retour au début de la page

    Similar models

    Baseline Signs And Symptoms for Screening

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    identification number
    Item
    Volunteer panel number
    integer
    C1300638 (UMLS CUI [1])
    Subject number
    Item
    Subject number
    integer
    C2348585 (UMLS CUI [1])
    Item Group
    Non-serious Adverse Event
    C1518404 (UMLS CUI-1)
    Non-serious Adverse Event
    Item
    Were baseline events experienced during the module?
    boolean
    C1518404 (UMLS CUI [1])
    Baseline sign symptom
    Item
    Baseline sign/symptom
    text
    C0037088 (UMLS CUI [1])
    Onset Date
    Item
    Onset Date
    date
    C2985916 (UMLS CUI [1])
    Onset Time
    Item
    Onset Time
    time
    C0449244 (UMLS CUI [1,1])
    C1518404 (UMLS CUI [1,2])
    End Date
    Item
    End Date
    date
    C2697886 (UMLS CUI [1])
    End Time
    Item
    End Time
    time
    C1518404 (UMLS CUI [1,1])
    C1522314 (UMLS CUI [1,2])
    Item
    Outcome
    integer
    C1705586 (UMLS CUI [1])
    Outcome
    Code List
    Outcome
    CL Item
    Resolved (1)
    CL Item
    Ongoing (2)
    CL Item
    Died (3)
    Item
    Event course
    integer
    C0877248 (UMLS CUI [1,1])
    C0750729 (UMLS CUI [1,2])
    Experience Course
    Code List
    Event course
    CL Item
    Intermittent (1)
    CL Item
    Constant (2)
    Number of episodes
    Item
    No. of episodes
    integer
    C0877248 (UMLS CUI [1,1])
    C4086638 (UMLS CUI [1,2])
    Item
    Intensity (maximum)
    integer
    C1710066 (UMLS CUI [1])
    Intensity
    Code List
    Intensity (maximum)
    CL Item
    Mild (1)
    CL Item
    Moderate (2)
    CL Item
    Severe (3)
    Item
    Relationship to study procedures performed prior to randomisation
    integer
    C0008976 (UMLS CUI [1,1])
    C2700391 (UMLS CUI [1,2])
    Relationship to Investigational Drug
    Code List
    Relationship to study procedures performed prior to randomisation
    CL Item
    Not related (1)
    CL Item
    Unlikely  (2)
    CL Item
    Suspected  (3)
    CL Item
    Probable (4)
    Item
    Corrective Therapy
    text
    C0877248 (UMLS CUI [1,1])
    C0087111 (UMLS CUI [1,2])
    Corrective Therapy
    Code List
    Corrective Therapy
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Item
    Was patient withdrawn due to this specific AE?
    text
    C0422727 (UMLS CUI [1,1])
    C1518404 (UMLS CUI [1,2])
    patient withdrawn due to this specific AE
    Code List
    Was patient withdrawn due to this specific AE?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Investigator signature
    Item
    Investigator signature:
    text
    C2346576 (UMLS CUI [1])
    Date
    Item
    Date:
    date
    C0011008 (UMLS CUI [1])
    Retour au début de la page 

    Contact

    Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

    Les champs marqués d’un * sont obligatoires.

    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