Ultrasound may fine-tune fluid balance in dialysis patients — a trial puts it to the test
NCT ID NCT07721636
First seen Jul 23, 2026 · Last updated Jul 24, 2026 · Updated 1 time
Summary
This study tests whether using lung ultrasound and the VExUS score can improve how doctors assess fluid status and set the ideal dry weight in people on maintenance hemodialysis. Forty adults with end-stage kidney disease will first be managed with standard clinical exams for 12 weeks, then with ultrasound-guided assessments for another 12 weeks. The goal is to see if ultrasound leads to a more accurate dry weight compared to the standard approach.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ultrasound-based volume assessment (POCUS, lung ultrasound, VExUS score)
- What this could lead to
- If successful, this approach could help dialysis patients achieve a more accurate dry weight, potentially reducing complications from fluid overload or dehydration.
- What could go wrong
- This is a small, single-center study with only 40 participants. The ultrasound technique may not be widely applicable or may not improve outcomes over standard care.
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 40 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- Lead sponsor
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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
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25 to 65 years
- 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: * ESRD patients on maintenance HD for more than three months. * In the HD unit at the Medical Research Institute and Faculty of Medicine. Alexandria University. * Age: 25 -65 years old. * The ability to give informed consent. Exclusion Criteria: * Patients with previous echocardiographic evidence of right heart dysfunction, tricuspid valve disease, or IVC thrombosis. * Patients with liver cirrhosis * Lung diseases: interstitial lung diseases, COPD patients. * Obese (BMI≥30)
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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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Alexandria University Hospitals
RECRUITINGAlexandria, Egypt
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