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Effect of Obesity on Extracellular Matrix Composition (EOBECM)

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University of Copenhagen

Status

Enrolling

Conditions

Adipose Tissue

Treatments

Other: Cross sectional study

Study type

Interventional

Funder types

Other

Identifiers

NCT06304506
514-0894/23-3000

Details and patient eligibility

About

The experiment is a simple cross-sectional study with three groups (n=10) in each group, young and old healthy men and obese young men. The study will investigate the composition of the adipose tissue extra cellular matrix.

The main questions to answer,

  • is there differences in the adipose tissue extracellular matrix in obese compared to young men is there differences in the adipose tissue extracellular matrix in old compared to young men

Full description

Three groups of young (n=10) and old (n=10) healthy men and obese young (n=10) men are recruited.

After verbal and written information is provided signed consent is obtained.

Subjects arrive at the lab overnight fasted and not having done exercise the prior day and having consumed a normal isocaloric carbohydrate rich diet.

After a voiding and a 15 min rest body composition is determined by DXA. After this blood pressure is measured in the supine position in triplicate separated by 1 min. Following this a venous blood sample is obtained from a cubital vein, and kept on ice until further handling.

Subsequently an adipose tissue biopsy is obtained by the Bergström technique applied with suction from an incision 3-5 cm lateral from the umbilicus. After compression and a 30 min rest, the subject perform an incremental exercise test to determine maximal fat oxidation. In brief pulmonary oxygen uptake and carbon dioxide excretion is measured using a COSMED Quark B2 on-line system during 5 min rest sitting on a cycle ergometer, and then during exercise with 3 min increments starting at 60 Watt and increasing by 35 watts. When the respiratory exchange ratio is above 1 the exercise is stopped. After a 5 min break an incremental test until voluntary exhaustion is performed to determine maximal oxygen uptake. This completes the experiment.

Enrollment

30 estimated patients

Sex

Male

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy men aged [18,35] and BMI [20,25]
  • Obese men aged [18,35] and BMI [30,40]
  • Healthy older men aged [60,75] and BMI [20,25]

Exclusion criteria

  • Present or former cardiovascular disease and chronical inflammatory disease
  • Consumption of medications and supplements that influence substrate use at rest and/or during exercise

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 3 patient groups

Young obese men
Experimental group
Description:
BMI \[30, 40\] Age \[18, 35\]
Treatment:
Other: Cross sectional study
Young healthy men
Experimental group
Description:
BMI \[20, 25\] Age \[18, 35\]
Treatment:
Other: Cross sectional study
Old healthy men
Experimental group
Description:
BMI \[20, 25\] Age \[60, 75\]
Treatment:
Other: Cross sectional study

Trial contacts and locations

1

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Central trial contact

Christoffer Clemmensen, PhD; Jørn Wulff W Helge, PhD

Data sourced from clinicaltrials.gov

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