Can simple samples predict transplant success? new study aims to unlock clues for Longer-Lasting organs
NCT ID NCT03997253
First seen Jun 29, 2026 · Last updated Jun 30, 2026 · Updated 1 time
Summary
This study follows 430 adults who have received a kidney, liver, or heart transplant to understand what factors help transplanted organs survive longer. Researchers collect blood, urine, and bile samples at several time points over the first year after transplant. The goal is to find early signs of rejection and improve long-term care for transplant recipients.
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 successful, this research could identify markers to predict transplant rejection and extend the life of transplanted organs, improving long-term outcomes for recipients.
- What could go wrong
- This is an observational study, not a treatment trial. It may not directly lead to new therapies, and findings may take years to translate into clinical practice.
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 430 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2020
- Expected to finish
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Jun 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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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: * Male or female over 18 (no age limit) * affiliated to a social security organization * Recipient (s) of a kidney, liver or heart transplant * followed by at least one of the FHU SUPORT centers (Tours, Poitiers, Limoges, Rennes) * having given informed consent to participate in the cohort. Exclusion Criteria: * Patient unable to understand the information given by the investigator * People under the protection of justice
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Genom att skicka in godkänner du våra Användarvillkor
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
4 sites. 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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Limoges hospital
RECRUITINGLimoges, France
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Poitiers Hospital
RECRUITINGPoitiers, 86000, France
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Rennes Hospital
NOT_YET_RECRUITINGRennes, 35000, France
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Tours hospital
RECRUITINGTours, 37000, France
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