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 @ 11:18 PM
Ignite Modification Date:
2025-12-24 @ 11:18 PM
NCT ID:
NCT05642156
Eligibility Criteria:
Inclusion Criteria:
* Written consent of the participant after being informed
* At least 18 years of age
* End stage kidney disease patient undergoing hemodialysis
* Dry weight stable for a minimum of one month
* Interdialytic weight gain of \>2 liters in the short interdialytic interval
Exclusion Criteria:
* No informed consent was obtained
* Patients with a pacemaker or implanted medical device that prevents compliance with study regulations
* Patients treated with hemodiafiltration
* Patients treated with medium cut-off membranes (Theranova, Baxter)
* Patients with recurrent severe hyperkalemia after the short interdialytic interval (K+ concentration \> 6.0 mmol/L, requiring more than 2 hours of dialysis to ameliorate the post-dialytic shift from other compartments.
* Women of childbearing age not using contraception
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT05642156
Study Brief:
Protocol Section:
NCT05642156