ID

30858

Beschrijving

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.

Link

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

Trefwoorden

  1. 27-06-18 27-06-18 - Sarah Riepenhausen
Houder van rechten

GlaxoSmithKline

Geüploaded op

27 juni 2018

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :


Geen commentaren

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

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

Pharmacogenetic Research (PGx)

Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Identifier
Beschrijving

Subject Identifier

Datatype

text

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

Consent for PGx Research (DNA)

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

Consent for Pharmacogenetic Research

Datatype

text

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

Date of consent for Pharmacogenetic Research

Datatype

date

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

Reason no consent for Pharmacogenetic research

Datatype

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
Beschrijving

Other Reason no consent for Pharmacogenetic research

Datatype

text

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

Sample Collection

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

Sample for Pharmacogenetic research

Datatype

text

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

Date sample taken

Datatype

date

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

Withdrawal of consent

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Has subject withdrawn consent for PGx research?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

Withdrawal of consent for pharmacogenetic research

Datatype

text

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

Date of consent withdrawal

Datatype

date

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

Sample Destruction

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

Request for sample destruction

Datatype

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:
Beschrijving

Reason for sample destruction request

Datatype

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
Beschrijving

Other Reason for sample destruction request

Datatype

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

Similar models

Pharmacogenetic Research (PGx)

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
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])
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])
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])
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])
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])
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])
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])
Code List
Other reason, specify

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