Recruiting NA Bloodpressure

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Official title Effects of Endogenous GIP on Postprandial Blood Pressure in Healthy Individuals

ClinicalTrials.gov ID: NCT06934473

What this study is testing

What it's testing
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.
  • You might receive a placebo (an inactive treatment) instead of the study drug, decided by chance. You may not know which one you got.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 to 40. Healthy volunteers may be eligible.

You may be able to join if

  • Age 18-40 years
  • BMI between 18.5 and 29.9 kg/m2 (both included)
  • Informed consent

You likely can't join if

  • Allergy or intolerance to ingredients included in the mixed meal
  • History of Orthostatic Hypotension (OH) or Postural Orthostatic Tachycardia Syndrome (POTS) or other autonomic dysfunction at the discretion of the...
  • Anaemia (haemoglobin below normal range \<7.3 mmol/L for women and \<8.3 mmol/L for men)
  • Kidney disease (estimated glomerular filtration rate (eGFR) \<90 ml/min/1.73 m2) at screening
  • Known liver disease and/or elevated plasma alanine aminotransferase (ALT) \> three times the upper limit of normal at screening
  • Treatment with antihypertensives
See the full eligibility criteria
Who can join
  • Age 18-40 years
  • BMI between 18.5 and 29.9 kg/m2 (both included)
  • Informed consent
What rules you out
  • Allergy or intolerance to ingredients included in the mixed meal
  • History of Orthostatic Hypotension (OH) or Postural Orthostatic Tachycardia Syndrome (POTS) or other autonomic dysfunction at the discretion of the investigators
  • Anaemia (haemoglobin below normal range \<7.3 mmol/L for women and \<8.3 mmol/L for men)
  • Kidney disease (estimated glomerular filtration rate (eGFR) \<90 ml/min/1.73 m2) at screening
  • Known liver disease and/or elevated plasma alanine aminotransferase (ALT) \> three times the upper limit of normal at screening
  • Treatment with antihypertensives
  • Treatment with GLP-1RA (Glucagon-like Peptide-1 Receptor Agonist)
  • Treatment with SNRI (Serotonin and Noradrenalin Reuptake Inhibitor) or treatment within two weeks before the first experimental day
  • Any ongoing medication that the investigator evaluates would interfere with trial participation
  • Any physical or psychological condition that the investigator evaluates would interfere with trial participation, including any acute or chronic illnesses
  • Any concomitant disease or treatment that, at the discretion of the investigators, might jeopardize the participant's safety during the trial
  • Alcohol/drug abuse as per discretion of the investigators
  • Pregnancy or breastfeeding
  • Participation in any other clinical trial during the study period
  • Mental incapacity or language barriers that preclude adequate understanding or cooperation or unwillingness to comply with trial requirements or pr discretion of the investigator

The study team makes the final eligibility decision.

Where it's taking place

  • Copenhagen, Hellerup, Denmark

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years to 40 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Copenhagen, Hellerup, Denmark. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.