Skip to main content
OpenTrials
Completed

NCT Number: NCT04337268

Acute Effects of GLP-1 on Renal Hemodynamics

This study investigates the hypothesis, that GLP-1's suppression of ANG II and natriuretic action increase medullary perfusion and decrease oxygen consumption, leading to higher tissue oxygenation.

Completed

Looking for future studies?

Notify Me

Key information

Age range

20 year–60 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Rigshospitalet - Glostrup

Glostrup Municipality, Copenhagen, 2600, Denmark

About this study

Human studies have recently demonstrated a significant natriuretic effect of GLP-1 when the extracellular fluid volume (ECFV) is expanded by intravenous sodium-loading; in these studies, there was a suppression of ANG II with no change in net renal hemodynamics, pointing to a tubular mechanism for reduced NaCl reabsorption secondary to the ANG II suppression. In the current randomized and controlled study, investigators aim to test the hypothesis that GLP-1's suppression of ANG II and natriuretic action increase medullary perfusion and decrease oxygen consumption, leading to higher tissue oxygenation. Thus, contributing to the renoprotective action of GLP-1.

Under fixed sodium intake for 4 days before each study day, 10 healthy male participants will be investigated during a 1-hour infusion of GLP-1 (1.5 pmol/kg/min) or vehicle together with an intravenous infusion of 0.9% NaCl. Interleaved measurements of RAF, oxygenation (T2*) and perfusion by arterial spin labeling in the renal cortex and medulla at fixed time points will be conducted, using Magnetic Resonance Imaging (MRI).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Normal health demonstrated by medical examination.
  • Normal values for fasting plasma glucose, total cholesterol, triglyceride, HDL, LDL, creatinine, AST, ALT and electrolyte concentrations.

Exclusion criteria

  • Immunosuppressive treatment for the previous 12 months.
  • Alcohol abuse.
  • Medical treatment with oral glucocorticoids, dipeptidyl peptidase-4 (DPP-4) inhibitors, or GLP-1 receptor agonists that, in the opinion of the investigator, may interfere with glucose metabolism.
  • Use of lithium.
  • Medical treatment that affects insulin secretion or cardiovascular efficacy goals.
  • Liver disease (ALT> 2 x normal value).
  • Renal impairment (creatinine> 130 µM and / or albuminuria).
  • Severe claustrophobia.
  • MRI incompatible foreign bodies.

Treatment and study plan

Glucagon-Like Peptide 1

Drug

Intravenous infusion (1.5 pmol/kg/min) for 60 min.

Other names: GLP-1

saline 0.9%

Drug

Intravenous infusion for 60 min.

Other names: Placebo for GLP-1

Primary outcomes

  1. T2* signal

    Time frame: 1 hour

    Changes in T2* signal in renal cortex and medulla

  2. Arterial Spin Labeled (ASL)

    Time frame: 1 hour

    Changes in Arterial Spin Labeled (ASL) MRI Perfusion Imaging in renal cortex and medulla

  3. Renal Artery Flow Phase (RAF)

    Time frame: 1 hour

    Changes in Renal Artery Flow Phase (RAF)-Contrast Magnetic Resonance

Sponsors and collaborators

Lead sponsor

Rigshospitalet, Denmark

Other

Collaborators

  • University of Southern Denmark

Registry information

Official study title

Acute Effects of GLP-1 on Renal Hemodynamics: Simultaneous Perfusion and Oxygenation Measurements in Cortex and Medulla Using Magnetic Resonance Imaging

Acronym: GLP1RRBF

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Apr 7, 2020
Registry last updated
Apr 7, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.