New Onset Diabetes After TransplantationPERCEIVENCT07512804
Post-Transplant Diabetes Outcomes Prediction
A study testing Whole genome sequencing (WGS) in people with New Onset Diabetes After Transplantation, run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS at 1 site in Italy.
Trial summary
Chronic Kidney disease (CKD) is a major global health burden and represents one of the most common non-communicable diseases. In Europe, CKD affects over 50 million people, representing approximately 10% of the adult population. Read more about this study
- Who is it for?
- Ages 18 to 70 years
- Conditions the study is for
- New Onset Diabetes After Transplantation
- What is being tested?
- Whole genome sequencing (WGS)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 120 participants
- Where
- 1 siteItaly
- Study dates
- 31 Aug 2024to 28 Feb 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- age between 18 and 70 years old,
- kidney graft recipients with a diagnosis of de novo post-transplant diabetes between 1 and 10 years from the time of enrollment,
- ability to sign a valid informed consent form.
Who cannot join
- diagnosis of neoplasia,
- the presence of an active infection,
- previous biopsy-proven diagnosis of a recurrent renal disease,
- NYHA class III-IV heart failure,
- hepatic failure.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Italy1 site, 1 recruiting
- Recruiting
Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Nefrologia
Roma, 00168
Giuseppe Grandaliano, +390630159983, giuseppe.grandaliano@unicatt.it
Giuseppe Grandaliano
About this study
Official title: Post-Transplant Diabetes Outcomes Prediction Through Machine Learning and Deep Phenotyping
Chronic Kidney disease (CKD) is a major global health burden and represents one of the most common non-communicable diseases. In Europe, CKD affects over 50 million people, representing approximately 10% of the adult population. Importantly, the presence of CKD is a significant economic burden on healthcare systems, with an estimated cost of 140 billion annually in Europe. Kidney transplantation represents the best treatment of end stage renal disease (ESRD) in terms of mortality, morbidity and quality of life. In addition, this therapeutic approach to ESRD considerably reduces the cost of renal replacement therapy. Post-transplant diabetes is a common metabolic complication of kidney transplantation. Up to 40% of kidney graft recipients present within the first 5 years after transplantation a diagnosis of de novo diabetes and another 30% are characterized by an impaired glucose tolerance (IGT). In addition, 20% of patients with IGT will eventually develop a post- transplant diabetes.
Immunosuppressive therapy represents the main culprit with its deleterious effects on either insulin resistance (corticosteroids, mTOR inhibitors) or insulin synthesis (tacrolimus). Behind the role of immunosuppressive therapy, other relevant risk factors are recipients' age and pre- and post-transplant BMI. A great amount of registry data and a recent meta- analysis on retrospective studies clearly indicate the detrimental effect of post-transplant diabetes on the main clinical outcome of kidney transplantation, recipients' mortality and graft loss. The excess mortality observed in this setting is mainly due, as expected, to an increase in cardiovascular death. Although the link between diabetes and cardiovascular mortality is well known and its mechanisms are mostly clear in the general population, we have a significant lack of information in this specific setting, where post- transplant diabetes act on the top of several other cardiovascular risk factors, often present in the transplant population. Thus, our ability to stratify the risk and to intervene accordingly, to prevent cardiovascular events in kidney graft recipients with post-transplant diabetes is significantly limited. This lack of knowledge will inevitably lead to an overtreatment of patients potentially at lower risk and to an under-treatment of graft recipients potentially at very high risk. On the other hand, when we consider the issue of graft loss, we inevitably focus our attention on the immunological mechanisms linked to the alloimmune response of the recipients against the graft and, subsequently on the modulation of immunosuppression. However, in the last few years we are realizing that the risk factor for ESRD that are well known in the general population have a significant prognostic weight also in the prediction of graft loss in kidney transplantation. We are well aware that among these risk factors the diabetes is still one of the most important. Although, also in this case we lack information on how the diabetic milieu interacts with transplant-specific ESRD risk factors to determine the fate of the graft.
In addition, for ESRD, our inability to stratify each patient risk will significantly limit our therapeutic intervention. Thus, the aim of the present project is to fill this gap of knowledge with an approach based on deep phenotyping of patients with post-transplant diabetes associated with a system biology strategy. This methodology will allow us to identify potential molecular markers at the urine, serum or renal tissue levels that will associate with clinical, imaging or histological features known to predict either cardiovascular mortality or ESRD. With the help of the artificial intelligence, we will then build the prototype of a predictive model for both cardiovascular mortality and graft loss to be then validated in a dedicated prospective study.
- Conditions
- New Onset Diabetes After Transplantation
- Being tested
- Whole genome sequencing (WGS)
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Whole genome sequencing (WGS)Genetic
Whole genome sequencing
| Study group | Role | What they receive |
|---|---|---|
| NEW ONSET DIABETES | Experimental | Whole genome sequencing on patients with new onset diabetes after transplantation Receives: Genetic: Whole genome sequencing (WGS) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Composite Diabetic Micro- and Macroangiopathy Assessed by Imaging and Graft Biopsy
The primary endpoint is a composite endpoint including any signs of diabetic micro and macro-angiopathy (presence of peripheral artery disease, myocardial perfusion defects, presence of retinopathy, presence and degree of neuropathy, extent of mesangial expansion, glomerulosclerosis, interstitial fibrosis and arterial hyalinosis at graft biopsy).
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Apr 2026
- Study start31 Aug 2024
- Primary completion28 Feb 2027 (estimated)
- Study completion28 Feb 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for New Onset Diabetes After TransplantationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 120 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, GRANDALIANO GIUSEPPE, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
- Investigators
- Giuseppe Grandaliano, Principal investigator, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07512804
- Sponsor's protocol ID
- 6828
- Acronym
- PERCEIVE
- Status last verified
- Mar 2026
- First submitted
- 27 Mar 2026
- Last updated
- 6 Apr 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Post-Transplant Diabetes Outcomes Prediction Through Machine Learning and Deep Phenotyping
- ClinicalTrials.gov ID
- NCT07512804
- Acronym / sponsor ID
- PERCEIVE / 6828
- Conditions
- New Onset Diabetes After Transplantation
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 120 participants (estimated)
- Lead sponsor
- Fondazione Policlinico Universitario Agostino Gemelli IRCCSUniversity, hospital or other
- Study start
- 31 Aug 2024 (actual)
- Primary completion
- 28 Feb 2027 (estimated)
- Study completion
- 28 Feb 2027 (estimated)
- First posted
- 6 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Chronic Kidney disease (CKD) is a major global health burden and represents one of the most common non-communicable diseases. In Europe, CKD affects over 50 million people, representing approximately 10% of the adult population. Importantly, the presence of CKD is a significant economic burden on healthcare systems, with an estimated cost of 140 billion annually in Europe. Kidney transplantation represents the best treatment of end stage renal disease (ESRD) in terms of mortality, morbidity and quality of life. In addition, this therapeutic approach to ESRD considerably reduces the cost of renal replacement therapy. Post-transplant diabetes is a common metabolic complication of kidney transplantation. Up to 40% of kidney graft recipients present within the first 5 years after transplantation a diagnosis of de novo diabetes and another 30% are characterized by an impaired glucose tolerance (IGT). In addition, 20% of patients with IGT will eventually develop a post- transplant diabetes.
Immunosuppressive therapy represents the main culprit with its deleterious effects on either insulin resistance (corticosteroids, mTOR inhibitors) or insulin synthesis (tacrolimus). Behind the role of immunosuppressive therapy, other relevant risk factors are recipients' age and pre- and post-transplant BMI. A great amount of registry data and a recent meta- analysis on retrospective studies clearly indicate the detrimental effect of post-transplant diabetes on the main clinical outcome of kidney transplantation, recipients' mortality and graft loss. The excess mortality observed in this setting is mainly due, as expected, to an increase in cardiovascular death. Although the link between diabetes and cardiovascular mortality is well known and its mechanisms are mostly clear in the general population, we have a significant lack of information in this specific setting, where post- transplant diabetes act on the top of several other cardiovascular risk factors, often present in the transplant population. Thus, our ability to stratify the risk and to intervene accordingly, to prevent cardiovascular events in kidney graft recipients with post-transplant diabetes is significantly limited. This lack of knowledge will inevitably lead to an overtreatment of patients potentially at lower risk and to an under-treatment of graft recipients potentially at very high risk. On the other hand, when we consider the issue of graft loss, we inevitably focus our attention on the immunological mechanisms linked to the alloimmune response of the recipients against the graft and, subsequently on the modulation of immunosuppression. However, in the last few years we are realizing that the risk factor for ESRD that are well known in the general population have a significant prognostic weight also in the prediction of graft loss in kidney transplantation. We are well aware that among these risk factors the diabetes is still one of the most important. Although, also in this case we lack information on how the diabetic milieu interacts with transplant-specific ESRD risk factors to determine the fate of the graft.
In addition, for ESRD, our inability to stratify each patient risk will significantly limit our therapeutic intervention. Thus, the aim of the present project is to fill this gap of knowledge with an approach based on deep phenotyping of patients with post-transplant diabetes associated with a system biology strategy. This methodology will allow us to identify potential molecular markers at the urine, serum or renal tissue levels that will associate with clinical, imaging or histological features known to predict either cardiovascular mortality or ESRD. With the help of the artificial intelligence, we will then build the prototype of a predictive model for both cardiovascular mortality and graft loss to be then validated in a dedicated prospective study.
Study design
- Primary purpose
- Prevention
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| NEW ONSET DIABETES | Experimental | Genetic: Whole genome sequencing (WGS)Whole genome sequencing on patients with new onset diabetes after transplantation |
Who may qualify
- Ages
- 18 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- age between 18 and 70 years old,
- kidney graft recipients with a diagnosis of de novo post-transplant diabetes between 1 and 10 years from the time of enrollment,
- ability to sign a valid informed consent form.
Key exclusion criteria (5 listed)
- diagnosis of neoplasia,
- the presence of an active infection,
- previous biopsy-proven diagnosis of a recurrent renal disease,
- NYHA class III-IV heart failure,
- hepatic failure.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Whole genome sequencing (WGS)Whole genome sequencing | Genetic | NEW ONSET DIABETES |
Primary outcome
Composite Diabetic Micro- and Macroangiopathy Assessed by Imaging and Graft Biopsy
Time frame: 6 months
The primary endpoint is a composite endpoint including any signs of diabetic micro and macro-angiopathy (presence of peripheral artery disease, myocardial perfusion defects, presence of retinopathy, presence and degree of neuropathy, extent of mesangial expansion, glomerulosclerosis, interstitial fibrosis and arterial hyalinosis at graft biopsy).
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Apr 2026.
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Cirrhosis, Liver, Diabetes Mellitus Risk
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Giuseppe Grandaliano principal investigator
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Whole genome sequencing (WGS) in people with New Onset Diabetes After Transplantation, run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS at 1 site in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 6 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Giuseppe Grandaliano (+390630159983, giuseppe.grandaliano@unicatt.it), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Composite Diabetic Micro- and Macroangiopathy Assessed by Imaging and Graft Biopsy (time frame: 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Apr 2026.