Skip to main content
OpenTrials
Completed

NCT Number: NCT05990933

Role of Adrenaline in in the Inflammatory Response in Diabetes

The primary aim of the present study is to study the effect of adrenaline administration on inflammatory parameters (e.g. leukocyte phenotype, cytokines, inflammatory proteins). Secondary objectives consist of the effect of adrenaline on atherogenic parameters.

* All participants will receive intravenous infusion of adrenaline for an hour * We will draw blood at 7 time points, not including screening * Participants will be asked to return for a total of 4 times

Researchers will compare 2 groups, healthy individuals versus people with diabetes type 1 to see if the inflammatory reaction to adrenaline differs between these two groups.

Completed

Looking for future studies?

Notify Me

Key information

Age range

16 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Radboud UMC

Nijmegen, Gelderland, 6525GA, Netherlands

About this study

Objective: The aim of the present study is to study the effect of increased adrenaline levels on the inflammatory response (e.g. leukocyte phenotype, cytokines, inflammatory proteins) by administering exogenous adrenaline in participants with type 1 diabetes and healthy participants.

Potentially eligible adult ( 16 - 75 years) participants will be recruited from the diabetes clinic at the department of internal medicine from the Radboud University Medical Center. Healthy participants will be recruited through social media and other advertisements. We will recruit a total of 30 individuals, i.e. 15 healthy participants and 15 people with type 1 diabetes. Participants with type 1 diabetes will be equipped with a blinded continuous glucose monitoring device (CGM) during the test, which will measure interstitial glucose levels for a total of 10 days.

Intervention: All participants will receive intravenous infusion of adrenaline at a rate of 0.04ug/kg/min for 1 hour. We will draw blood at baseline, 30 minutes, 60 minutes, 180 minutes, 24 hours 72 hours and a week after start of infusion. The blood samples will be used for phenotyping of the innate immune system and measuring inflammatory and atherogenic parameters. Throughout the infusion, vital parameters will be monitored.

Who can participate

Healthy volunteers accepted: Yes

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

Overall inclusion criteria:

  • Ability to provide written informed consent
  • Body-Mass Index: 19-30kg/m2
  • Age ≥16 years, ≤ 75 years
  • Blood pressure: <140/90 mmHg
  • Non-smoking
  • Electrocardiogram not showing any serious arrythmia's (PVC's and PAC's accepted)

Diabetes group specific criteria:

  • Insulin treatment according to basal-bolus insulin regimen (injections or insulin pump)
  • Duration of diabetes > 1 year
  • HbA1c < 100 mmol/mol,

Exclusion criteria

  • Any event of cardiovascular disease in the past 5 years (e.g. myocardial infarction, stroke, heart failure, symptomatic peripheral arterial disease)
  • Pregnancy or breastfeeding or unwillingness to undertake measures for birth control
  • Epilepsy
  • Current treatment with Alpha or beta blockers ( doxazosin, propranolol)
  • History of panic disorders
  • History of Arrhythmias
  • Use of immune-modifying drugs or antibiotics
  • Use of tricyclic antidepressants or MAO inhibitors
  • Use of statins (e.g. stop statins >2 weeks before performing blood sampling.
  • Any infection with systemic symptoms in past 2 weeks
  • Previous vaccination in the past 2 weeks
  • Proliferative retinopathy
  • Nephropathy with an estimated glomerular filtration rate (by MDRD) ˂60ml/min/1.73m2

Treatment and study plan

Adrenaline

Drug

Adrenaline infusion at a rate of 0.04ug/kg/min for 1 hour administered intravenously.

Other names: Adrenaline infusion

Primary outcomes

  1. Monocyte count

    Time frame: Change from baseline compared to after 1 hour

    The amount of monocytes following 60 minutes of adrenaline infusion compared to baseline to asses the adrenaline effect on the inflammatory response.

Secondary outcomes

  1. Leukocyte count

    Time frame: Change from baseline at day 30, 60 and 180 minutes 1, day 3 and day 7 after adrenaline infusion

    Measurement of the amount of leukocytes

  2. Leukocyte phenotype

    Time frame: Change from baseline at day 30, 60 and 180 minutes 1, day 3 and day 7 after adrenaline infusion

    Measuring several phenotypes by using a pre-defined panel of interest with flow-cytometry ( e.g. NK-cells, granulocytes)

  3. Pro-inflammatory proteins

    Time frame: Change from baseline at day 30, 60 and 180 minutes 1, day 3 and day 7 after adrenaline infusion

    Pro-inflammatory proteins using Olink Proteomics AB inflammation panel with 92 circulating inflammatory proteins ( e.g. EN-rage, FIT3L)

  4. Inflammation plasma parameters

    Time frame: Change from baseline at 30, 60 and 180 minutes day 1, day 3 and day 7 after adrenaline infusion

    Inflammatory plasma protein using ELISA, ( e.g high sensitive-crp)

  5. Atherogenic parameters

    Time frame: Change from baseline at 30, 60 and 180 minutes day 1, day 3 and day 7 after adrenaline infusion

    Atherogenic parameters using ELISA method including but not limited to, VCAM-1, ICAM-1, E-Selectin, P-selectin, PAI-1, Plasma Endothelin

  6. Insulin

    Time frame: Change from baseline at, 60 and 180 minutes

    Plasma levels of insulin

  7. Adrenaline

    Time frame: Change from baseline at 30, 60 and 180 minutes

    Plasma levels of adrenaline

  8. Noradrenaline

    Time frame: Change from baseline at 30, 60 and 180 minutes

    Plasma levels of noradrenaline

  9. Glucose variability

    Time frame: 2 weeks

    Glucose variability measured by the blinded continuous glucose monitor including but not limited to, measuring time within range, amount of hypoglycaemic events, amount of hyperglycaemic events.

  10. Ex vivo cytokines

    Time frame: Change from baseline at 30, 60 and 180 minutes, day 1, day 3 and day 7 after adrenaline infusion

    Ex vivo production of pro- and anti-inflammatory cytokines and chemokines after ex vivo stimulation of isolated monocytes, including TNF-α, IL-6, IL-10 and IL-1β.

  11. Distribution of monocyte subset

    Time frame: Change from baseline at 30, 60 and 180 minutes, day 1, day 3 and day 7 after adrenaline infusion

    Distribution of pro- and anti-inflammatory monocyte subsets using FACS (Fluorescence-activated Cell Sorting)

Sponsors and collaborators

Lead sponsor

Cees Tack

Other

Registry information

Official study title

Role of Adrenaline in the Inflammatory Response in People with Diabetes Mellitus Type 1, and Healthy Individuals

Acronym: RAID

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Aug 14, 2023
Registry last updated
Nov 21, 2024

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.

Published trials that share one or more normalized conditions with this study.