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RecruitingNCT07512804PERCEIVEUpdated Apr 6, 2026

Post-Transplant Diabetes Outcomes Prediction

An interventional study of Whole genome sequencing (WGS) in New Onset Diabetes After Transplantation, sponsored by Fondazione Policlinico Universitario Agostino Gemelli IRCCS. Recruiting at 1 site in Italy. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-04-06.

Sponsored by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 1 year 6 months after the study started (first participant enrolled Aug 2024, registered Mar 2026).
  • Started Aug 2024; still recruiting 2 years 1 month later.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
01

Study 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. 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.

02

Conditions studied

  • New Onset Diabetes After Transplantation
03

In context

Lead sponsor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS is the lead sponsor of 920 studies on the registry; 529 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 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.

Exclusion criteria

Exclusion Criteria:

  • 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.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    NEW ONSET DIABETES

    Whole genome sequencing on patients with new onset diabetes after transplantation

    Genetic: Whole genome sequencing (WGS)

Interventions

  • GeneticWhole genome sequencing (WGS)

    Whole genome sequencing

06

What researchers measure

Primary outcomes

  1. 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).

    Time frame: 6 months

07

Study locations

1 of 1 sites recruiting
  • Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Nefrologia
    Roma, 00168, Italy
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07512804
Lead sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Responsible party
GRANDALIANO GIUSEPPE (Professor, MD, Fondazione Policlinico Universitario Agostino Gemelli IRCCS) — Principal investigator
First posted
Apr 6, 2026
Start date
Aug 31, 2024
Primary completion
Feb 28, 2027 (estimated)
Completion
Feb 28, 2027 (estimated)
Last update
Apr 6, 2026

Study contacts

Giuseppe Grandaliano
Contact
giuseppe.grandaliano@unicatt.it
+390630159983
Giuseppe Grandaliano
principal investigator · Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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