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Co-infusion of Neurotensin and GLP-1 Effects on Appetite and Food Intake.

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University of Copenhagen

Status

Enrolling

Conditions

Obesity

Treatments

Other: GLP-1 + saline
Other: Saline + saline
Other: Neurotensin + saline
Other: GLP-1 + Neurotensin

Study type

Interventional

Funder types

Other

Identifiers

NCT04186026
514-0386/19-3000

Details and patient eligibility

About

Co-infusion of Neurotensin and GLP-1 Effects on Appetite and Food Intake.

Full description

Neurotensin (NT), a gut hormone and neuropeptide, and GLP-1, as well a gut hormone, increases in circulation after bariatric surgery in rodents and humans and inhibit food intake in mice.

Studies in rodents have shown that a GLP-1 receptor agonist and long acting neurotensin inhibit food intake.

This study investigates whether the synergistic anorexic effects of neurotensin and GLP-1 agonism suggested by animal studies can be translated.

Enrollment

35 estimated patients

Sex

Male

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Informed consent
  • Above 18 years of age
  • Normal hemoglobin concentration
  • 28<BMI<40 kg/m2

Exclusion criteria

  • Diabetes mellitus
  • Truncal vagotomy
  • Resection of intestine (apart from appendectomy)
  • Tobaccos use
  • Nephropathy (serum-creatinin>130 micromolar or/and albuminuria)
  • Liver disease (Alanine transaminase or/and aspartate transaminase>2 times normal range.)
  • Treatment with medication that cannot be paused in 12 hours
  • Allergy towards latex or plastic
  • Bleeding disorder

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

35 participants in 4 patient groups

Saline+Saline
Other group
Treatment:
Other: Saline + saline
Neurotensin+Saline
Other group
Treatment:
Other: Neurotensin + saline
GLP-1+Saline
Other group
Treatment:
Other: GLP-1 + saline
Neurotensin + GLP-1
Other group
Treatment:
Other: GLP-1 + Neurotensin

Trial contacts and locations

2

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Central trial contact

Birgitte Holst, PhD, Professor; Sten Madsbad, DMsc, Professor

Data sourced from clinicaltrials.gov

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