Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:34 AM
Ignite Modification Date:
2025-12-25 @ 1:34 AM
NCT ID:
NCT06553794
Eligibility Criteria:
Inclusion Criteria:
* Aged 18-35 years or 67+ years
* Body mass index (BMI) between 18.5 and 30 kg/m2
* Regular stool frequency ranging from 1-3 times/day
Exclusion Criteria:
* History of cardiovascular, respiratory, gastrointestinal, urogenital, neurological, psychiatric, dermatologic, musculoskeletal, metabolic, endocrine, haematological, immunologic disorders, allergy, major surgery and/or laboratory assessments which might limit participation in or completion of the study protocol, interfere with the execution of the experiment, or potential influence the study outcomes (to be decided by the principal investigator and responsible physician)
* Major abdominal surgery interfering with gastrointestinal function (upon judgement of the principal investigator and responsible physician)
* Use of medication which limit participation in or completion of the study protocol, interferes with the execution of the experiment, or potential influences the study outcomes (to be decided by the principal investigator and responsible physician)
* Use of supplementation (i.e. protein, vitamin, pre- and probiotic supplementation) within 14 days prior to testing
* Administration of investigational drugs or participation in any scientific intervention study prior or during the study, which may interfere with this study (upon judgement of the principal investigator and responsible physician) Specific diet (e.g. vegetarian, vegan, gluten free, no diary) within the study period
* Planning to lose weight during the study period
* Excessive alcohol consumption (defined as \> 14 alcoholic consumptions per week)
* Smoking
* Drug use
* Pregnancy
* Lactation
* Donated blood three months prior to the test day
* No given permission to register participation in electronic patient file at MUMC+ and to add records of gastroduodenoscopy
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06553794
Study Brief:
Protocol Section:
NCT06553794