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 @ 2:15 AM
Ignite Modification Date:
2025-12-25 @ 2:15 AM
NCT ID:
NCT04954560
Eligibility Criteria:
Inclusion Criteria:
* Age 18 years old
* Fulfillment of three or more of the AHA / NHLBI 2005 assessment criteria for the metabolic syndrome:
* abdominal obesity (i.e. handling in women ≥88 cm) male ≥ 102 cm
* concentration of triglycerides in the form ≥150 mg / dl
* concentration of HDL fraction (men \<40 mg / dL, women \<50 mg / dL)
* blood pressure ≥ 130/85 mmHg
* Correction of fasting glucose ≥100 mg / dL)
* Written and informed consent to participate in the case of
Exclusion Criteria:
* Congenital defects in fructose metabolism (hereditary fructose intolerance and idiopathic fructosuria)
* Mental illness, dementia
* Insufficient cooperation with the patient, non-compliance with doctor's recommendations
* Pregnancy
* Bilateral renal artery stenosis or stenosis to a solitary kidney and other contraindications for angiotensin receptor antagonists
* Chronic use of uricosuric drugs, xanthine oxidase inhibitors and AT1 receptor inhibitors
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT04954560
Study Brief:
Protocol Section:
NCT04954560