Viewing Study NCT06487832



Ignite Creation Date: 2024-07-17 @ 11:31 AM
Last Modification Date: 2024-10-26 @ 3:34 PM
Study NCT ID: NCT06487832
Status: RECRUITING
Last Update Posted: 2024-07-05
First Post: 2024-06-27

Brief Title: Effect of GLP1 Receptor Agonist on Brain Insulin Responsiveness
Sponsor: University Hospital Tuebingen
Organization: University Hospital Tuebingen

Study Overview

Official Title: Impact of the Incretin System on Brain Insulin Sensitivity in Humans With Normal Weight Overweight and Obesity
Status: RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The overarching goal of the current study is to investigate the effect of GLP-1 on brain insulin responsiveness in a randomized single-blinded within subject cross-over study design To this end investigators will compare the effect of the administration of semaglutide versus placebo followed by an fMRI with administration of intranasal insulin or placebo
Detailed Description: Investigate the effect of the GLP1 receptor agonist ie 025 mg semaglutide vs placebo on the brain using functional magnetic resonance imaging fMRI in combination with 160IU intranasal insulin vs placebo administration in healthy male and female participants of normal-weight and overweightobesity Participants will furthermore undergo tasks that assess cognitive functions and eating behavior Brain insulin responsiveness primary outcome is defined as the cerebral response to intranasal insulin compared to placebo by means of cerebral blood flow and resting-state BOLD measurements Secondary outcomes include diffusion weighted imaging neural food cue reactivity cognitive functions and metabolic predictors

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None