Postprandial Profiles of Metabolites and Appetite-regulating Hormones in Plasma and Cerebrospinal Fluid
NCT ID: NCT06115304
Last Updated: 2023-11-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
30 participants
INTERVENTIONAL
2023-10-05
2024-10-10
Brief Summary
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The purpose of this health science research project is to describe the coinciding plasma and cerebrospinal fluid (CSF) profiles of selected biomarkers after co-ingestion of a meal and model pharmaceuticals in patients with overweight and/or type 2 diabetes compared to healthy control individuals.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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Intervention arm
Large liquid meal, spinal catheter and venous line
Large liquid meal (e.g. Nutricia® Energy 500 ml (750 kcal) admixed paracetamol 1000 mg (for estimation of gastric emptying).
Spinal catheter for 4 hours, with samples taken at one hour interval.
2 venous lines, one for saline and one for venous sampling every half hour
Interventions
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Large liquid meal, spinal catheter and venous line
Large liquid meal (e.g. Nutricia® Energy 500 ml (750 kcal) admixed paracetamol 1000 mg (for estimation of gastric emptying).
Spinal catheter for 4 hours, with samples taken at one hour interval.
2 venous lines, one for saline and one for venous sampling every half hour
Eligibility Criteria
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Inclusion Criteria
* 10 male volunteers with normal weight (BMI 20-24) matched by age
* 10 male volunteers with obesity (BMI \>30) matched by age
Exclusion Criteria
2. Hepatic disease or hemorrhagic diatheses (including abnormal International Normalized Ratio (INR), bilirubin, blood levels of thrombocytes, alanine-aminotransferase (ALAT))
3. Anticoagulant treatment (e.g. treatment with warfarin, apixaban or another oral anticoagulant)
4. Anaemia (p-hemoglobin below normal range)
5. Nephropathy (se-creatinine \>130 μM and/or albuminuria)
6. Suspected difficult access to the spinal canal (e.g. pronounced scoliosis, spinal stenosis, osteoporotic coincidence in the lower back, spina bifida, meningocele after surgical intervention)
7. Lumbar skin infection (e.g. herpes zoster, pustules or ulcers)
8. Medical history with headaches - both in connection with dura puncture and frequent headaches of other types
9. Central nervous system disease (including dementia, previous stroke, multiple sclerosis, epilepsy, etc.)
10. Clinical suspicion of increased intracranial pressure (headaches, visual disturbances etc.)
11. Patients with type 2 diabetes: Treatment with DPP-4 inhibitor or GLP-1 receptor agonist. Late diabetic complications including proliferative diabetic retinopathy (anamnestic), arteriosclerotic cardiovascular disease (heart failure or previous ischemic event/myocardial infarction)
50 Years
70 Years
MALE
Yes
Sponsors
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Mikkel Bring Christensen
OTHER
Responsible Party
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Mikkel Bring Christensen
Chief consultent at the department of Clinical Pharmacology
Principal Investigators
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[email protected] B Christensen, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Department of clinical pharmacology, Bispebjerg Hospital
Locations
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Deparrtment of clinical pharmacology
Copenhagen, , Denmark
Countries
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Central Contacts
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Facility Contacts
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Mikkel B Christensen, MD, PhD
Role: primary
Other Identifiers
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CSF-meal
Identifier Type: -
Identifier Source: org_study_id
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