ClinicalTrials.Veeva

Menu

PET-study on the Role of the Reward System in Weight Loss After Bariatric Surgery (ObesiPET)

U

University Medical Center Groningen (UMCG)

Status

Enrolling

Conditions

Obesity

Treatments

Other: standardized liquid mixed meal Nutridrink®

Study type

Interventional

Funder types

Other

Identifiers

NCT05359887
UMCG202100632

Details and patient eligibility

About

Bariatric surgery (BS) is currently the most effective treatment in severe obesity. However, a considerable percentage of patients undergoing BS fail to lose sufficient weight or regain weight after initial weight loss during long-term follow-up, which may be attributed to personality traits and pathological eating behaviour. Previous positron emission tomography (PET) studies have shown reduced dopamine D2 receptor availability in obese patients and upregulation of this availability following successful BS in the brain's reward system. Dopamine D2 receptor availability in patients with unsuccessful BS has not been investigated to date.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Bariatric surgery 24-36 months prior to the study
  • Adult (over 18y old)
  • Mentally capable to understand the consequences of the procedure and make his or her own choice without coercion
  • Able to undergo PET and MRI, according to the investigator's assessment
  • Native speaking
  • Able to participate in follow-up
  • Written informed consent

Exclusion criteria

  • Presence of a DSM-IV axis 1 disorder
  • The use of drugs that bind to dopamine D2/3 receptors, including various classes of antipsychotics and antidepressants
  • History of stroke, brain tumor, Parkinson's Disease or dementia
  • History of head trauma with loss of consciousness
  • Alcohol or substance abuse in the last 6 months
  • Alcohol consumption 24h prior to PET scanning
  • Smoking or other forms of nicotine intake 12 hours prior to PET scanning
  • Use of anorectic drugs in the last 6 months
  • Current pregnancy
  • Medication for Diabetes Mellitus
  • Claustrophobia
  • The presence of implanted metal objects of the type which may concentrate radiofrequency fields or cause tissue damage from twisting in a magnetic field (such as certain implanted devices, shrapnel, ocular metal shavings)
  • Patients with a bodyweight > 200kg will be excluded to ensure the maximum load of the camera bed of the PET-scanner (227 kg) is not exceeded.

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Unsuccessful BS (Total Weight Loss (TWL) < 20%)
Experimental group
Description:
Fifteen who had unsuccessful BS (Total Weight Loss (TWL) \< 20%)
Treatment:
Other: standardized liquid mixed meal Nutridrink®
Successful BS (TWL > 25%).
Experimental group
Description:
Fifteen who had successful BS (TWL \> 25%).
Treatment:
Other: standardized liquid mixed meal Nutridrink®

Trial contacts and locations

1

Loading...

Central trial contact

Andre P. van Beek, MD PhD; D.L. Marinus Oterdoom, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems