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the Bispebjerg Study of Diurnal Variations

the Bispebjerg Study of Diurnal Variations

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06166368
Acronym
DIURNAL
Enrollment
24
Registered
2023-12-12
Start date
2008-10-11
Completion date
2009-01-01
Last updated
2023-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diurnal

Brief summary

To evaluate the influence of time of day on the circulating concentrations of various biochemical markers in healthy men

Interventions

OTHERDiurnal variation

Venous blood samples were obtained under standardized circumstances from 24 healthy young men every third hour through 24 hours, nine time points in total.

Sponsors

University of Copenhagen
CollaboratorOTHER
Bispebjerg Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Medically healthy * Normal sleep-wake pattern

Exclusion criteria

* acute or chronic medical diseases * had worked nightshifts the last 14 days before the study * transatlantic traveling the last 14 days before the study * had been smoking the last 14 days before the study * had an irregular sleep-wake pattern, * didn't sleep 7-8 hours pr night * were extreme morning- or evening types, * had plasma hemoglobin \< 8.0 mmol/L * ody mass index (BMI) \<18.5 kg/m2 or \>24.9 kg/m2.

Design outcomes

Primary

MeasureTime frameDescription
hematology parameters24 hoursComposite measurement of hematological measurements

Secondary

MeasureTime frame
Plasma Levels of Glucagon24 hours
Plasma levels of GLP-124 hours
Plasma levels of GIP24 hours
Plasma levels of c-peptide24 hours
Plasma levels of glucose24 hours

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026