Obesity Trial, Recruiting NCT06874309 Sponsor: Masaryk University Condition: Obesity
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Obesity Trial, Recruiting

NCT06874309
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have severe or morbid obesity, meaning a BMI over 35 or 40 kg/m², and who meet current medical guidelines for bariatric (weight-loss) surgery.
  • People who show signs of reduced control over their eating habits, as measured by a specific questionnaire called the Eating Habits Questionnaire.

Who may not be able to join:

  • People who are not able to give informed consent, or who are unable to understand or take part in study procedures, as determined by the treating doctor.
  • People who have a personal history of heart disease caused by blocked arteries, heart attack, stroke, heart failure, or an irregular heart rhythm called atrial fibrillation.
  • People who have already had bariatric (weight-loss) surgery in the past.
  • People who are pregnant or who plan to become pregnant during the study period.
  • People considered unsuitable for the study following assessment by a specialist, such as a doctor or neuropsychologist.
  • People who have dreadlocks, as this can interfere with the EEG (brainwave monitoring) equipment used in the study.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 20 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Irena Rektorová, Prof., Cetral European Institute of Technology

Phone: +420 776 722 029

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Masaryk University
Registry
ClinicalTrials.gov
Start date
1 May 2024
Est. completion
31 December 2026

Where this trial is recruiting

🇨🇿 Czechia

Primary endpoints

Cognitive impulse control measured via food-modified Go/No-Go task

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov