Empagliflozin for Peritoneal and Kidney Function in End Stage Renal Disease
This study is looking at how a medication called empagliflozin (25 mg or 10 mg) affects people with End Stage Renal Disease (ESRD) who are on peritoneal dialysis (PD). The main goal is to see if empagliflozin can reduce how much sugar (glucose) is absorbed in your belly (peritoneum). You might be able to join if you are over 18, have been on PD for more than 3 months, and have a working PD catheter. People with certain types of diabetes or frequent low blood sugar are not able to join. This study is currently unclear about its recruitment status and plans to enroll about 30 participants.
- Study design
- This is a randomized, placebo-controlled study with an initial crossover phase, followed by an open-label extension. About 30 participants will be involved.
- What's involved
- You will have three main study visits and up to four safety visits over nine weeks. You will take empagliflozin or a placebo, and undergo a PET test at each visit.
- Compensation
- Not stated in the trial record.
- Follow-up
- The primary endpoint, glucose absorption, is measured from Day 0 to Day 63.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Effect of Empagliflozin on Peritoneal and Kidney Function in End Stage Renal Disease
At a glance
Conditions
NCT05671991
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Yale University
New Haven, Connecticutno site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Jeffrey Testani, MD · PRINCIPAL_INVESTIGATOR · Yale University
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
What this trial measures
- Glucose absorption with empagliflozin vs. placeboDay 0 to Day 63
Total glucose absorption in grams with empagliflozin vs. placebo