Can cutting unnecessary pills improve kidney patient health?
NCT ID NCT06324045
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This trial tests whether a team of doctors and pharmacists can safely reduce the number of unnecessary medications taken by people with chronic kidney disease in Qatar. 424 patients will be randomly assigned to receive the deprescribing program or usual care. The goal is to see if this approach lowers the use of risky medications and improves quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- deprescribing program (medication review and reduction plan)
- What this could lead to
- If successful, this could show that a structured deprescribing program safely reduces medication burden and improves quality of life for people with chronic kidney disease.
- What could go wrong
- This is a relatively small, single-country trial testing a behavioral intervention, not a drug. Results may not apply to other settings, and deprescribing carries risks if medications are stopped inappropriately.
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
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 424 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2024
- Expected to finish
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Mar 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: Patients who are: * diagnosed with ESRD receiving hemodialysis treatment or pre-dialysis patients who are followed up at a low clearance clinic. * receiving treatment at one of the ambulatory kidney centers in Qatar for at least two months. * able to communicate in Arabic and/or English. Exclusion Criteria: * Unstable or has a psychiatric condition. * Presents with uncontrolled behaviors or exit-seeking behaviors (i.e., seeking to leave the premises out of confusion, frustration, or anger). * Critically ill patients, pregnant women, children, mentally ill, dementia, and unconscious patients. * Patients with limited life expectancy (less than 6 months).
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hamad Medical Corporation
RECRUITINGDoha, 3050, Qatar
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