Postprandial Profiles of Metabolites and Appetite-regulating Hormones in Plasma and Cerebrospinal Fluid

NCT ID: NCT06115304

Last Updated: 2023-11-03

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-10-05

Study Completion Date

2024-10-10

Brief Summary

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Overweight and obesity are rising in prevalence and becoming a growing threat to public health. Obesity is associated with an increased all-cause mortality, impaired quality of life, and numerous of disorders. Therapeutic strategies against obesity - which include an abundance of dietary and physical training programmes and pharmaceutical drugs to increase energy expenditure or limit appetite or gastro-intestinal fat absorption - have shown limited success on long term weight loss. Thus, overweight and associated conditions is becoming the new normal and there is a need for better understanding gut-to-brain signalling, hormonal and metabolic disturbances in overweight individuals.

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.

Detailed Description

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Conditions

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Obesity Diabetes Mellitus, Type 2

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Intervention arm

Group Type OTHER

Large liquid meal, spinal catheter and venous line

Intervention Type OTHER

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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 10 male patients with obesity (BMI \>30) and type 2 diabetes
* 10 male volunteers with normal weight (BMI 20-24) matched by age
* 10 male volunteers with obesity (BMI \>30) matched by age

Exclusion Criteria

1. Unwillingness to participate or wish to withdraw from ongoing protocol
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)
Minimum Eligible Age

50 Years

Maximum Eligible Age

70 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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Mikkel Bring Christensen

OTHER

Sponsor Role lead

Responsible Party

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Mikkel Bring Christensen

Chief consultent at the department of Clinical Pharmacology

Responsibility Role SPONSOR_INVESTIGATOR

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

Site Status RECRUITING

Countries

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Denmark

Central Contacts

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Mikkel B Christensen, MD, PhD

Role: CONTACT

+4538635102

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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