Clinical Trials Logo

Hyperkalaemia clinical trials

View clinical trials related to Hyperkalaemia.

Filter by:
  • Completed  
  • Page 1

NCT ID: NCT05462119 Completed - Hyperkalaemia Clinical Trials

Safety of Oral Resin for Treatment of Hyperkalemia in Chinese Patients With Renal Insufficiency

SCRUTINIZE
Start date: August 22, 2022
Phase:
Study type: Observational

It is a multicenter, prospective, non-interventional cohort study, in order to evaluate the safety of oral resin for treatment of hyperkalemia in Chinese patients with renal insufficiency.

NCT ID: NCT05271266 Completed - Hyperkalaemia Clinical Trials

A Multicenter, Prospective, Non-interventional Cohort Study to Evaluate the Safety and Treatment Pattern of Sodium Zirconium Cyclosilicate for Hyperkalaemia Management in Real World Practice in China

ACTUALIZE
Start date: March 22, 2022
Phase:
Study type: Observational

The study is a multi-center prospective (primary data) non-interventional cohort study which enrolls 1500 patients including new and ongoing users on SZC at Study Enrollment Day in real-world clinical practice. The eligible study patients will be identified by physicians in each study site by assessing the patients or reviewing the medical record. The prescription (including initiation, dose-adjusting or interruption) or discontinuation of SZC will be determined by physicians as per real-world clinical practice and in accordance with the local label. Any AZ employee, or member of the research operation team must not intervene in the decision-making of any physician or patient through any approach, at any time during the study. Every patient will be followed up according to standard clinical practice for 6 months from enrolment.

NCT ID: NCT04788641 Completed - Hyperkalaemia Clinical Trials

Study to Assess the Effect of Sodium Zirconium Cyclosilicate on the Pharmacokinetics of Tacrolimus and Cyclosporin in Healthy Subjects

Start date: March 30, 2021
Phase: Phase 1
Study type: Interventional

This study will be an open-label, randomised sequence, 2-period, 2-cohort, 2-treatment in each cohort, cross-over study in healthy subjects (males and females of non-childbearing potential), performed at a single study centre.