Status:

NOT_YET_RECRUITING

The Effect of Glucagon on Cerebral Glucose Metabolism in Healthy Humans

Lead Sponsor:

Nicolai Jacob Wewer Albrechtsen

Collaborating Sponsors:

Department of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital - Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark

Conditions:

Cerebral Glucose Metabolism

Eligibility:

All Genders

55-70 years

Phase:

NA

Brief Summary

This is a pilot study in which the investigators will investigate the effect of exogenous glucagon on cerebral glucose metabolism in healthy humans. Participants will participate in either part C or ...

Detailed Description

Participants in this study will participate in four visits; one screening visit and three study days. Participants will be instructed to avoid strenuous exercise and alcohol intake two days prior to ...

Eligibility Criteria

Inclusion

  • Age 55 to 70 years
  • BMI under or equal to 30 kg/m2
  • Capable of understanding the participant information and signing the consent form

Exclusion

  • Enrolment in other research projects that might interfere with the study
  • Diabetes diagnosis (type 1 and 2)
  • Use of medications which, in the opinion of the investigator, may jeopardise participant's safety or compliance with the protocol
  • Diagnosis of psychiatric disorders, dementias, or any other neurological disorders that in the opinion of the investigator precludes compliance with the study protocol, evaluation of the results or represents an unacceptable risk for the participants safety
  • Severe claustrophobia
  • Impaired liver og kidney function
  • Cardiac problems including any of the following:
  • Classified as being in New York Heart Association (NYHA) class III or IV
  • Angina pectoris (chest pain) within the last 6 months
  • Acute myocardial infarction (heart attack) within last 2 years
  • Inadequately treated blood pressure at screening defined as repeated resting blood pressure outside the range 90-150 mmHg for systolic and 50-100 mmHg for diastolic.
  • Active or recent malignant disease
  • Current or history of severe alcohol use or drug/chemical abuse as per investigator's judgement
  • Any chronic disorders or severe diseases which, in the opinion of the investigator, might jeopardise participant's safety or compliance with the protocol

Key Trial Info

Start Date :

March 1 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

March 1 2026

Estimated Enrollment :

12 Patients enrolled

Trial Details

Trial ID

NCT06877208

Start Date

March 1 2025

End Date

March 1 2026

Last Update

March 24 2025

Active Locations (1)

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Department of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital - Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark

Copenhagen, Denmark, 2400