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Microdialysis and Jugular Bulb Glucose Profiles During Hyperglycaemic Clamping in Patients With Severe Acute Brain Injury

Microdialysis and Jugular Bulb Glucose Profiles During Hyperglycaemic Clamping in Patients With Severe Acute Brain Injury

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06393049
Acronym
CLAMP
Enrollment
14
Registered
2024-05-01
Start date
2024-05-08
Completion date
2025-12-31
Last updated
2026-02-25

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

Conditions

Acute Brain Injury

Keywords

Acute brain injury, Intensive care, Neurointensive care, Anaesthesiology, Multimodal neuromonitoring, Glucose, Hyperglycaemic clamp

Brief summary

Acute brain injury is a serious condition that often results in admission to an intensive care unit. Some of the most seriously ill patients are fitted with multimodal neuromonitoring, a newer monitoring modality that can, among other things, measure oxygen tension and sugar levels in brain tissue. It is common clinical practice, but the interaction between the body's sugar levels and the brain's sugar levels is not sufficiently elucidated. The study will investigate the relationship between the body's sugar levels, measured in arterial and venous blood, and the brain's sugar level, measured by microdialysis, in patients with severe acute brain injury. Furthermore, we hope to be able to use our measurements to set up a mathematical model for the brain's sugar uptake.

Interventions

Following an overnight fast, the investigators will perform simultaneous samples from the arterial line, the venous line, and microdialysis and consider these samples as baseline values. If the patient's blood glucose level is at 8-10 mmol/L at baseline, the investigators will not proceed with the intervention and instead evaluate if the intervention can take place the following day. After baseline values are measured, intravenous glucose 20% (200g/1,000 ml) is infused to raise the glucose levels in both plasma and extravascular glucose compartments with approximately 3 mmol/L.

Sponsors

Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

14 patients, all will have an hyperglycaemic clamp performed during admission while measuring cerebral microdialysis

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years. * Admission to the neuro-ICU at Rigshospitalet. * Multimodal neuromonitoring

Exclusion criteria

* Closest relative does not understand written and spoken Danish or English. * Patients with known diabetes mellitus upon admission.

Design outcomes

Primary

MeasureTime frameDescription
(Change in) MD-glucose (mmol/L)Throughout the intervention, approximately five hoursChange in) MD-glucose (mmol/L) over time as a function of (a set change in) arterial blood glucose (mmol/L)

Secondary

MeasureTime frameDescription
Jugular vein glucose (mmol/L) over time as a function of arterial blood glucose.Throughout the intervention, approximately five hoursJugular vein glucose (mmol/L) over time as a function of arterial blood glucose (mmol/L)
Lactate-pyruvate-ratio (LP-ratio) as a function of arterial blood glucose.Throughout the intervention, approximately five hours.Two other microdialysis paramethers, lactate and pyruvat, will be assessed to evaluate the lactate-pyruvate ratio over time as a function of arteriel blood glucose.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026