Phase
Condition
Hypertriglyceridemia
Obesity
Treatment
N/AClinical Study ID
Ages 18-70 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Group 1 (Lean): BMI 18.5-22.0 kg/m², reporting difficulty gaining weight
Group 2 (Obese): BMI >30 kg/m², reporting difficulty losing weight
Healthy status as determined by medical history, physical examination, andlaboratory tests
Stable weight (less than 5% fluctuation) over the past 6 months
Exclusion
Exclusion Criteria:
Prediabetes (HbA1c >5.6% or fasting blood glucose >100 mg/dL) or diabetes mellitus
Conditions affecting appetite or energy expenditure (e.g., Cushing's syndrome,uncontrolled hyper-/hypothyroidism)
Gastrointestinal disorders that impact nutrient absorption (e.g., inflammatory boweldisease, malabsorption syndromes, ulcers)
Psychiatric conditions influencing eating behavior (e.g., active depression,anorexia nervosa, bulimia nervosa, borderline personality disorder)
Acute, unstable cardiovascular disease requiring hospitalization within the last 6months (e.g., stent placement)
Cancer that required treatment in the past 5 years
Chronic kidney disease (Stage IV or higher, per NKF criteria)
Active infectious disease (e.g., HIV, hepatitis)
Current nicotine use or nicotine use within the last month prior to screening
Illicit drug use (e.g., amphetamines, cocaine, heroin, marijuana)
Regular high-intensity physical activity (≥1 hour/day)
Non-MRI-compatible metallic implants (e.g., artificial joints, metal plates)
Pregnancy or breastfeeding
Use of weight-loss medications
Clinically significant claustrophobia
Any other condition not mentioned above that, in the opinion of the investigator,could interfere with study participation or compromise patient safety
Study Design
Study Description
Connect with a study center
University Hospital Schleswig-Holstein
Kiel, Schleswig-Holstein 24105
GermanyActive - Recruiting
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