Examination of How the Duration of Fasting and Temporary Stopping of GLP-1 Medications Affect the Amount of Food Left in the Stomach in People Using Liraglutide (Injected), Semaglutide (Taken by Mouth) or Semaglutide (Injected)

ConditionObesity
Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorNovo Nordisk A/S

About this trial

The purpose of this study is to investigate how the duration of fasting and temporary stopping of Glucagon-Like-Peptide 1 (GLP-1) medications affect the amount of food left in the stomach in people using liraglutide (injected), semaglutide (taken by mouth) or semaglutide (injected). The length of participants participation in the study will depend on the type of GLP-1 RA treatment participants are already using.

Eligibility criteria

Qualifiers

None

Disqualifiers

Previous dosing in this study.

Previous rescreening for this study.

Female who is pregnant, breast-feeding or intends to become pregnant or is of childbearing potential and not using adequate contraceptive method

Current participation (i.e., signed informed consent) in any other interventional clinical study.

Trial design

Treatments tested in this trial

  • Liraglutide
  • Oral Semaglutide
  • Semaglutide

Treatment groups

75 Participants
are divided into 3 treatment groups

Sponsors and collaborators