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ID

30858

Description

This ODM file contains Pharmacogenetic (PGx) Research Information. Study ID: 109710 Clinical Study ID: DAN109710 Study Title: A single-blind, randomized, placebo controlled, two-period crossover fMRI study to investigate the effects of the D3 antagonist GSK598809 on neural and behavioural responses to food reward and reinforcement after a single oral dose of GSK598809 in overweight and obese subjects. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01039454 https://clinicaltrials.gov/ct2/show/NCT01039454 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GSK598809 Trade Name: Study Indication: Substance Dependence Brief Summary: This novel compound is a new experimental treatment that may help people to stop compulsive overeating. Compulsive overeating or binge eating is one of the main reasons why people are overweight or obese. Recent research has shown that some kinds of overeating may be linked to a brain chemical called dopamine. There is some evidence that blocking the action of this chemical in animals can reduce food intake, particularly of foods that are high in fat and sugar. The purpose of this study is to find out if this compound (which blocks the effects of dopamine) has the same effect in overweight or obese people, as it does in animals.

Lien

https://clinicaltrials.gov/ct2/show/NCT01039454

Mots-clés

Versions (1)
  1. 27/06/2018 27/06/2018 - Sarah Riepenhausen
Détendeur de droits

GlaxoSmithKline

Téléchargé le

27 juin 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
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    Effects of D3 antagonist GSK598809 on neural and behavioural responses to food reward/reinforcement after a single dose in overweight/obese subjects NCT01039454

    Anglais

    Pharmacogenetic Research (PGx)

    1 Formulaires  
    Administrative Data
    Description

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Identifier
    Description

    Subject Identifier

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2348585
    Consent for PGx Research (DNA)
    Description

    Consent for PGx Research (DNA)

    Alias
    UMLS CUI-1
    C0021430
    UMLS CUI-2
    C2347500
    Has informed consent been obtained for PGx research?
    Description

    Consent for Pharmacogenetic Research

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C2347500
    If Yes, record the date informed consent obtained for PGx research
    Description

    Date of consent for Pharmacogenetic Research

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C0031325
    UMLS CUI [1,2]
    C0021430
    UMLS CUI [1,3]
    C0011008
    If No, pick one reason:
    Description

    Reason no consent for Pharmacogenetic research

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0031325
    UMLS CUI [1,2]
    C0021430
    UMLS CUI [1,3]
    C0392360
    Other Reason for no consent for PGx research, specify
    Description

    Other Reason no consent for Pharmacogenetic research

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0031325
    UMLS CUI [1,2]
    C0021430
    UMLS CUI [1,3]
    C0392360
    UMLS CUI [1,4]
    C0205394
    Sample Collection
    Description

    Sample Collection

    Alias
    UMLS CUI-1
    C0005834
    UMLS CUI-2
    C0031325
    Has a sample been collected for PGx research?
    Description

    Sample for Pharmacogenetic research

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0005834
    UMLS CUI [1,2]
    C0031325
    If Yes, record the date sample taken
    Description

    Date sample taken

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C1302413
    UMLS CUI [1,2]
    C0031325
    Withdrawal of consent
    Description

    Withdrawal of consent

    Alias
    UMLS CUI-1
    C1707492
    UMLS CUI-2
    C0031325
    Has subject withdrawn consent for PGx research?
    Description

    Withdrawal of consent for pharmacogenetic research

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C1707492
    UMLS CUI [1,2]
    C0031325
    If Yes, record the date informed consent withdrawn for PGx research
    Description

    Date of consent withdrawal

    Type de données

    date

    Alias
    UMLS CUI [1,1]
    C1707492
    UMLS CUI [1,2]
    C0011008
    UMLS CUI [1,3]
    C0031325
    Sample Destruction
    Description

    Sample Destruction

    Alias
    UMLS CUI-1
    C1948029
    UMLS CUI-2
    C0178913
    UMLS CUI-3
    C0031325
    Has a request been made for sample destruction?
    Description

    Request for sample destruction

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C1272683
    UMLS CUI [1,2]
    C1948029
    UMLS CUI [1,3]
    C0178913
    UMLS CUI [1,4]
    C0031325
    If Yes, pick one reason:
    Description

    Reason for sample destruction request

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0566251
    UMLS CUI [1,2]
    C1272683
    UMLS CUI [1,3]
    C1948029
    UMLS CUI [1,4]
    C0178913
    UMLS CUI [1,5]
    C0031325
    Other reason, specify
    Description

    Other Reason for sample destruction request

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0566251
    UMLS CUI [1,2]
    C1272683
    UMLS CUI [1,3]
    C1948029
    UMLS CUI [1,4]
    C0178913
    UMLS CUI [1,5]
    C0031325
    UMLS CUI [1,6]
    C0205394
    Retour au début de la page

    Similar models

    Pharmacogenetic Research (PGx)

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Item
    Subject Identifier
    text
    C2348585 (UMLS CUI [1])
    Visit
    Code List
    Subject Identifier
    Item Group
    Consent for PGx Research (DNA)
    C0021430 (UMLS CUI-1)
    C2347500 (UMLS CUI-2)
    Item
    Has informed consent been obtained for PGx research?
    text
    C0021430 (UMLS CUI [1,1])
    C2347500 (UMLS CUI [1,2])
    Relative Time
    Code List
    Has informed consent been obtained for PGx research?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Date of consent for Pharmacogenetic Research
    Item
    If Yes, record the date informed consent obtained for PGx research
    date
    C0031325 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    C0011008 (UMLS CUI [1,3])
    Item
    If No, pick one reason:
    text
    C0031325 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    C0392360 (UMLS CUI [1,3])
    Reason no consent for Pharmacogenetic research
    Code List
    If No, pick one reason:
    CL Item
    Subject declined (1)
    CL Item
    Subject not asked by investigator (2)
    CL Item
    Other (Z)
    Other Reason no consent for Pharmacogenetic research
    Item
    Other Reason for no consent for PGx research, specify
    text
    C0031325 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    C0392360 (UMLS CUI [1,3])
    C0205394 (UMLS CUI [1,4])
    Item Group
    Sample Collection
    C0005834 (UMLS CUI-1)
    C0031325 (UMLS CUI-2)
    Item
    Has a sample been collected for PGx research?
    text
    C0005834 (UMLS CUI [1,1])
    C0031325 (UMLS CUI [1,2])
    Sample for Pharmacogenetic research
    Code List
    Has a sample been collected for PGx research?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Date sample taken
    Item
    If Yes, record the date sample taken
    date
    C1302413 (UMLS CUI [1,1])
    C0031325 (UMLS CUI [1,2])
    Item Group
    Withdrawal of consent
    C1707492 (UMLS CUI-1)
    C0031325 (UMLS CUI-2)
    Item
    Has subject withdrawn consent for PGx research?
    text
    C1707492 (UMLS CUI [1,1])
    C0031325 (UMLS CUI [1,2])
    Relative Time
    Code List
    Has subject withdrawn consent for PGx research?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Date of consent withdrawal
    Item
    If Yes, record the date informed consent withdrawn for PGx research
    date
    C1707492 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    C0031325 (UMLS CUI [1,3])
    Item Group
    Sample Destruction
    C1948029 (UMLS CUI-1)
    C0178913 (UMLS CUI-2)
    C0031325 (UMLS CUI-3)
    Item
    Has a request been made for sample destruction?
    text
    C1272683 (UMLS CUI [1,1])
    C1948029 (UMLS CUI [1,2])
    C0178913 (UMLS CUI [1,3])
    C0031325 (UMLS CUI [1,4])
    Relative Time
    Code List
    Has a request been made for sample destruction?
    CL Item
    Yes (Y)
    CL Item
    No (N)
    Item
    If Yes, pick one reason:
    text
    C0566251 (UMLS CUI [1,1])
    C1272683 (UMLS CUI [1,2])
    C1948029 (UMLS CUI [1,3])
    C0178913 (UMLS CUI [1,4])
    C0031325 (UMLS CUI [1,5])
    Reason for sample destruction request
    Code List
    If Yes, pick one reason:
    CL Item
    Subject withdrew consent for PGx (3)
    CL Item
    Screen failure (2)
    CL Item
    Other (Z)
    Item
    Other reason, specify
    text
    C0566251 (UMLS CUI [1,1])
    C1272683 (UMLS CUI [1,2])
    C1948029 (UMLS CUI [1,3])
    C0178913 (UMLS CUI [1,4])
    C0031325 (UMLS CUI [1,5])
    C0205394 (UMLS CUI [1,6])
    Reason for sample destruction request
    Code List
    Other reason, specify
    Retour au début de la page 

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