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:
2025-12-24 @ 2:52 PM
Ignite Modification Date:
2025-12-24 @ 2:52 PM
NCT ID:
NCT02166359
Eligibility Criteria:
Inclusion Criteria:
* PD patients agree with written informed consent
* Incident and prevalent PD patients on dialysis for at least 3month
* PD patients treated with two glucose solutions including 2.5% or 4.25% dextrose solution at least 4hour
Exclusion Criteria:
* PD patients with allergy to starch-based polymers
* PD patients with glycogen storage disease
* PD patients with maltose or isomaltose intolerance
* PD patients with active alcohol/substance abuse
* Pregnant or nursing PD patients
* PD patients with an episode of peritonitis and active systemic infection within 4weeks before study initiation
* PD patients newly prescribed with lipid-lowering medications, including statins, omega-3 fatty acids or sevelamer hydrochloride within 3 months before randomization
* PD patients with triglyceride level\> 500 mg/dL/L or \<100 mg/dL
* PD patients with albumin level \< 3.0 gram/dL
* PD patients treated with automated PD
* PD patients had been treated or are treating with icodextrin PD solutions
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
20 Years
Maximum Age:
80 Years
Study:
NCT02166359
Study Brief:
Protocol Section:
NCT02166359