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 @ 4:17 AM
Ignite Modification Date:
2025-12-25 @ 4:17 AM
NCT ID:
NCT02558920
Eligibility Criteria:
Inclusion Criteria for controlled trials:
* Randomized and non-randomized controlled intervention studies in humans
* Oral fructose-containing sugars intervention
* Presence of a reduced fructose-containing sugars comparator in one of 4 energy controlled designs (substitution, addition, subtraction, or ad libitum)
* Diet duration \>=2 weeks
* Viable outcome data
Inclusion Criteria for prospective cohort studies:
* Prospective cohort studies
* Duration \>= 1 year
* Assessment of the exposure of food sources of fructose-containing sugars
* Ascertainment of viable outcome data by level of exposure
Exclusion Criteria for controlled trials:
* Observational studies or intervention studies with no control group
* IV or parenteral fructose-containing sugars intervention
* Lack of an adequate comparator (i.e. lack of a difference (\<5 g) in fructose-containing sugars between the intervention and control diets)
Exclusion Criteria for prospective cohort studies:
* Ecological, cross-sectional, or retrospective observational studies
* Intervention studies
Healthy Volunteers:
True
Sex:
ALL
Study:
NCT02558920
Study Brief:
Protocol Section:
NCT02558920