ID
30550
Beschreibung
This ODM file contains a checklist for Completion of Questionnaires to be filled at the mentioned times during Session visits 1 and 2 (Day 1 each). 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
Stichworte
Versionen (2)
- 13.06.18 13.06.18 - Sarah Riepenhausen
- 09.07.18 09.07.18 - Sarah Riepenhausen
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
13. Juni 2018
DOI
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Lizenz
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
Questionnaire Checklist (Sessions 1+2)
- StudyEvent: ODM
Beschreibung
Pre-Dose and 2h post-dose Questionnaires
Alias
- UMLS CUI-1
- C0439565
- UMLS CUI-2
- C0034394
- UMLS CUI-3
- C0439572
Beschreibung
To be filled for both timepoints
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0439564
- UMLS CUI [1,2]
- C0034394
Beschreibung
Bond and Lader VAS
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0681889
- UMLS CUI [1,2]
- C0026516
Beschreibung
Appetite VAS
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0003618
- UMLS CUI [1,2]
- C3536884
Beschreibung
Distress VAS
Datentyp
text
Alias
- UMLS CUI [1,1]
- C3536884
- UMLS CUI [1,2]
- C0231303
Beschreibung
Barnes Akathisia Scale
Datentyp
text
Alias
- UMLS CUI [1]
- C3541345
Beschreibung
Simpson Angus EPS Scale
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0681889
- UMLS CUI [1,2]
- C0041755
- UMLS CUI [1,3]
- C0015371
Beschreibung
Abnormal Involuntary Movement Scale
Datentyp
text
Alias
- UMLS CUI [1]
- C0450978
Beschreibung
4 and 10 h post-dose Questionnaires
Alias
- UMLS CUI-1
- C0034394
- UMLS CUI-2
- C0439574
- UMLS CUI-3
- C0439568
- UMLS CUI-4
- C0040223
Beschreibung
5, (8), 24 hrs post-Dose questionnaires
Alias
- UMLS CUI-1
- C0439568
- UMLS CUI-2
- C0040223
- UMLS CUI-3
- C0034394
Beschreibung
At 8 hrs post-dose only neccessary if abnormal at 5 hrs post-dose. 5 and 24 hrs post-dose mandatory.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0439564
- UMLS CUI [1,2]
- C0034394
Beschreibung
"X" only if not neccessary at 8 hrs post dose.
Datentyp
text
Alias
- UMLS CUI [1]
- C3541345
Beschreibung
"X" only if not neccessary at 8 hrs post dose.
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0681889
- UMLS CUI [1,2]
- C0041755
- UMLS CUI [1,3]
- C0015371
Beschreibung
"X" only if not neccessary at 8 hrs post dose.
Datentyp
text
Alias
- UMLS CUI [1]
- C0450978
Ähnliche Modelle
Questionnaire Checklist (Sessions 1+2)
- StudyEvent: ODM
C0034394 (UMLS CUI-2)
C0439572 (UMLS CUI-3)
C0026516 (UMLS CUI [1,2])
C3536884 (UMLS CUI [1,2])
C0231303 (UMLS CUI [1,2])
C0041755 (UMLS CUI [1,2])
C0015371 (UMLS CUI [1,3])
C0439574 (UMLS CUI-2)
C0439568 (UMLS CUI-3)
C0040223 (UMLS CUI-4)
C0231303 (UMLS CUI [1,2])
C0040223 (UMLS CUI-2)
C0034394 (UMLS CUI-3)
C0034394 (UMLS CUI [1,2])
C0041755 (UMLS CUI [1,2])
C0015371 (UMLS CUI [1,3])