tissues and organs
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthy volunteer: - Disease currently not requiring prescription medication - Baseline venous glucose level below 11.0 mmol/L - Age >= 18 years - Signed and dated written informed consent prior to any study-specific procedures Patient: - WHO performance status of 0 or 1 - Baseline venous glucose level below 11.0 mmol/L - Age >= 18 years - Signed and dated written informed consent prior to any study-specific procedures
Exclusion criteria
Exclusion criteria: Healthy volunteer: - Glucose infusion related exclusion criteria: * Diabetes Mellitus type 1 or 2 (self-reported or 2 measurements on separate days of a non-fasting glucose level >11 mmol/L or fasting glucose level >=7,0 mmol/L) * Sickle cell disease or blood iron deficiency (haemoglobin concentration =11.0 mmol/L or a fasting glucose level >=7.0 mmol/L) * Sickle cell disease or blood iron deficiency, with haemoglobin concentration
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To optimize a glucoCEST protocol for MRI of the brain in healthy volunteers and patients with brain tumours. | — |
Secondary
| Measure | Time frame |
|---|---|
| Test-retest reliability will be determined. | — |
Countries
Netherlands