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TOlerance MOlecular and Genome-wide Studies With Renal Allograft Recipient Material

TOlerance MOlecular and Genome-wide Studies With Renal Allograft Recipient Material

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05124444
Acronym
TOMOGRAM
Enrollment
18
Registered
2021-11-18
Start date
2015-08-22
Completion date
2021-09-29
Last updated
2021-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kidney Transplantation

Brief summary

TOMOGRAM is a European multicentric, prospective, experimental, controlled study that aims to increase our understanding of the causative mechanisms of operational tolerance in kidney transplantation through the achievement of several multimodal whole-genomic analysis in human biological samples.

Interventions

GENETICHigh throughput DNA and RNA sequencing

High throughput DNA and RNA sequencing

Sponsors

DESCARTES Working Group On Transplantation
CollaboratorOTHER
Université Libre de Bruxelles
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

1. Exome-wide association study 2. Transcriptomic analyses

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* recipient of an allogenic renal allograft, * have experienced (whatever ongoing or not) at least a whole year with blood creatinine \<1.7 mg/dL and proteinuria \</=1g/day or /g creatinine despite the COMPLETE discontinuation of immunosuppressive drugs, * alternatively, have experienced (whatever ongoing or not) at least a whole year with stable blood creatinine (max 20% variation) and proteinuria above these criteria despite the COMPLETE discontinuation of immunosuppressive drugs

Exclusion criteria

* Past medical history of allogeneic bone-marrow transplantation / combined organ transplantation

Design outcomes

Primary

MeasureTime frame
Number of moderately to highly damaging exonic variantsThrough study completion, an average of 2 year

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026