Can a software platform and blood test speed kidney transplant recovery?
NCT ID NCT07825688
First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time
Summary
Researchers are studying whether a software platform called TxAccess, which helps transplant centers, kidney doctors, and dialysis clinics share information, can improve recovery for patients whose new kidney is slow to work, a condition called delayed graft function. The study also uses a blood test called donor-derived cell-free DNA to check for kidney injury. About 450 adults who recently had a deceased donor kidney transplant and experienced delayed graft function will take part. The goal is to see if these tools reduce time on dialysis and improve immune outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- TxAccess software platform and donor-derived cell-free DNA blood test
- What this could lead to
- If it works, this could help transplant teams coordinate care faster and spot early signs of kidney injury, potentially reducing dialysis time and hospital stays for patients with delayed graft function.
- What could go wrong
- This is an observational study without a control group, so it cannot prove cause and effect. The platform's success depends on adoption by busy clinics, and the blood test may not reliably predict outcomes in all patients.
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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 450 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2029
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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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.
Study Population: Patients Inclusion criteria: Adult patients who experienced delayed graft function after a deceased donor kidney transplant in the last 2 calendar years Exclusion criteria: Patients younger than 18 years old at the time of transplant; patients who experienced graft loss prior to discharge from their index hospitalization patients who receive outpatient dialysis at a center that does not utilize TxAccess (intervention period) Study Population: Clinicians Inclusion criteria: adult clinicians who participate in care of kidney transplant recipients, including surgeons, nephrologists, pharmacists, social workers, nurse coordinators, advanced practice providers, nurses, case managers and dialysis center clinicians and staff. Exclusion criteria: clinicians and staff who are not employed at participating centers or do not have direct patient contact or experience with care coordination
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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 official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
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Other studies related to the condition(s) this trial covers.
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