Tiny study tests diuretics for dialysis patients – terminated early
NCT ID NCT05915286
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This pilot study tested two diuretics (furosemide and chlorthalidone) in people on dialysis who still had some kidney function. The goal was to see if these water pills could help preserve remaining kidney function, increase urine output, and reduce weight gain between dialysis sessions. Only 2 participants were enrolled, and the study was terminated early, so no firm conclusions can be drawn.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Furosemide and chlorthalidone (water pills)
- What this could lead to
- If it works, this could point toward a way to help dialysis patients keep some kidney function and reduce fluid buildup between treatments.
- What could go wrong
- This was a very small pilot study (only 2 participants) that was terminated early, so results are not reliable. It is too early to know if diuretics are safe or effective for dialysis patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
2 people
The number who actually took part.
- Started
-
May 2023
- Finished
-
Feb 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patients (age 18 years or older), who are within their first 12 months of chronic (expected to need dialysis for at least 6 months), in-centre hemodialysis therapy, and * Residual renal function defined as 24-hour urine volume \>200cc, and * Life expectancy of at least 6 months, and * Participants must be able to understand the consent process and be able to sign a consent form or have a substitute decision maker who is able to understand and sign consent on their behalf. In the case of non-English speaking participants, a translator service will be used to provide study information and obtain consent. Exclusion Criteria: * Unable to complete baseline urine collection * Documented allergy or adverse reaction to furosemide or chlorthalidone. * Unable to take oral medications * Patients expecting to change modality (peritoneal dialysis, home dialysis) or to receive a renal transplant in the next 6 weeks * History of hypokalemia (\<3.0 mmol/L), hypomagnesemia (\<0.6mmol/L), or hypocalcaemia (\<1.9mmol/L) in preceding 2 weeks. * Already participating in another study and one of the studies could interfere with the other study * Use of loop, or thiazide diuretic medications in the last week (if a patient is on chronic diuretics, they would need to be discontinued for 1 week before starting the trial)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Alberta
Edmonton, Alberta, T6G 2B7, Canada
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