Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
NCT06934473

Effects of Endogenous GIP on Postprandial Blood Pressure in Healthy Individuals

Led by University Hospital, Gentofte, Copenhagen · Updated on 2025-09-08

16

Participants Needed

2

Research Sites

36 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The present study investigates the postprandial role of endogenous glucose-dependent insulinotropic polypeptide (GIP) on cardiovascular haemodynamics, hormone responses, and hypotensive symptoms during a tilt test.

CONDITIONS

Official Title

Effects of Endogenous GIP on Postprandial Blood Pressure in Healthy Individuals

Who Can Participate

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 40 years
  • Body mass index (BMI) between 18.5 and 29.9 kg/m2
  • Provided informed consent
Not Eligible

You will not qualify if you...

  • Allergy or intolerance to ingredients in the mixed meal
  • History of orthostatic hypotension, postural orthostatic tachycardia syndrome, or other autonomic dysfunction
  • Anaemia with hemoglobin below normal range (<7.3 mmol/L for women, <8.3 mmol/L for men)
  • Kidney disease with estimated glomerular filtration rate (eGFR) <90 ml/min/1.73 m2
  • Known liver disease or elevated plasma alanine aminotransferase (ALT) over three times the upper limit of normal
  • Treatment with antihypertensive drugs
  • Treatment with GLP-1 receptor agonists
  • Treatment with serotonin and noradrenalin reuptake inhibitors or treatment within two weeks before first experimental day
  • Use of any ongoing medication that may interfere with participation
  • Any physical or psychological condition interfering with participation, including acute or chronic illnesses
  • Any disease or treatment that might endanger safety during the trial
  • Alcohol or drug abuse
  • Pregnancy or breastfeeding
  • Participation in another clinical trial during the study period
  • Mental incapacity, language barriers, or unwillingness to comply with trial requirements

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Center for Clinical Metabolic Research

Copenhagen, Hellerup, Denmark, 2900

Not Yet Recruiting

2

Center for Clinical Metabolic Research

Copenhagen, Hellerup, Denmark, 2900

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

4

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