Plastics in dialysis: could they add toxins to Children's blood?
NCT ID NCT07763483
First seen Aug 13, 2026 · Last updated Aug 18, 2026 · Updated 3 times
Summary
This study looks at whether children with chronic kidney disease, especially those on dialysis, have higher levels of PFAS chemicals in their blood. PFAS are found in many everyday products and may interfere with bone development. The study compares PFAS levels in children with kidney disease who are not on dialysis, those on peritoneal dialysis, and those on hemodialysis. It also checks if PFAS levels change during a hemodialysis session. The goal is to see if dialysis equipment, which contains plastics, might contribute to PFAS exposure in children.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Blood sample collection for PFAS measurement
- What this could lead to
- If this pilot shows that dialysis affects PFAS levels in children, it could lead to larger studies and eventually strategies to reduce exposure and protect bone health in young dialysis patients.
- What could go wrong
- This is a small pilot study with only 15 participants, so results may not apply broadly. It only measures PFAS levels, not direct health outcomes, and cannot prove cause and effect.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 15 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2028
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.
Who is studied
Participants will be recruited from the Pediatric Nephrology Department of the Femme-Mère-Enfant Hospital, Hospices Civils de Lyon. A total of 15 patients will be enrolled in the study, distributed as follows: * 3 children with non-dialysis chronic kidney disease (CKD) stages 1-2 * 3 children with non-dialysis chronic kidney disease (CKD) stages 4-5 * 3 children receiving peritoneal dialysis * 3 children receiving paediatric haemodialysis with pre-dilution hemodiafiltration * 3 children receiving paediatric haemodialysis with post-dilution hemodiafiltration.
- Ages
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2 to 17 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Children aged 0 to 17 years (inclusive), followed in the Paediatric Nephrology Department of the Femme-Mère-Enfant Hospital, Hospices Civils de Lyon. * No objection from the parents or legal guardian(s). * Assent of the minor participant, when appropriate according to age and level of understanding * For group 1: Children with non-dialysis chronic kidney disease (CKD) stages 1-2, weighing at least 5 kg. * For group 2: Children with non-dialysis chronic kidney disease (CKD) stages 4-5, weighing at least 5 kg. * For group 3: Children receiving peritoneal dialysis, weighing at least 5 kg. * For group 4: Children receiving paediatric haemodialysis with pre-dilution hemodiafiltration, weighing at least 12 kg. * For group 5: Children receiving paediatric haemodialysis with post-dilution hemodiafiltration, weighing at least 12 kg. Exclusion Criteria: * Participation in another interventional research study with an exclusion period still ongoing on the day of inclusion and deemed by the investigator to potentially interfere with the present study. * Individuals deprived of liberty by a judicial or administrative decision.
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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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Hôpital Femme-Mère-Enfant
Bron, 69500, France
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