Do kidney patients know why a fistula matters before dialysis?

NCT ID NCT07817953

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
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Running, but no longer taking on new participants.
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The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
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Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
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When the status isn't known

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First seen Sep 14, 2026 · Last updated Sep 15, 2026 · Updated 1 time

Summary

Researchers at Assiut University Hospital survey adults with advanced chronic kidney disease about arteriovenous fistula creation, the surgically connected vein and artery used for hemodialysis. The study includes pre-dialysis patients and people already on maintenance hemodialysis, who answer questions about fistula preparation, maturation time, arm protection, and how a fistula differs from a catheter. The goal is to measure how much patients know and how many received counseling before starting dialysis.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If the survey finds gaps in patient knowledge, hospitals could design better education programs so more people with kidney failure start dialysis with a proper fistula instead of a temporary catheter.
What could go wrong
This is a single-center questionnaire study with 116 participants, so its findings may not reflect patients elsewhere. It measures what people say they know, not whether better education actually improves dialysis outcomes.

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.

Participants

About 116 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Feb 2028

An estimate. End dates often move.

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.

Who is studied

Adults with advanced chronic kidney disease (CKD stage 4-5 not on maintenance hemodialysis or currently receiving maintenance hemodialysis) attending the Nephrology Unit and Maintenance Hemodialysis Unit of Assiut University Hospital.

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age 18 years or older * Documented chronic kidney disease * CKD stage 4-5 not on maintenance hemodialysis OR currently on maintenance hemodialysis for established CKD * Able to understand and answer the questionnaire * Written informed consent Exclusion Criteria: * Acute kidney injury without established CKD * Previous kidney transplantation (if considered to affect homogeneity) * Severe cognitive or communication impairment preventing reliable questionnaire completion * Unable or unwilling to provide informed consent * Inability to provide reasonably reliable information about the pre-dialysis period (for retrospective questions)

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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

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