Patients With Diabetes Mellitus on Drug Treatment on the List or Already Undergoing Orthotopic Liver Transplantation
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Diabetes Mellitus Type 2, Liver Transplant. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Italy
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Adult Patients With Diabetes Mellitus, on Drug Treatment, on the List or Already Undergoing Orthotopic Liver Transplantation: an Observational Study
Overview
observational study through which we aim to collect information on metabolic compensation, the degree of satisfaction with hypoglycemic therapy, the onset of complications of diabetes or liver disease, evaluation of survival, in patients on the list for at least three months or already undergoing liver transplantation for at least three months
Primary outcome measures
- glycosilated hemoglobin (%) [Time frame: through study completion, an average of 5 years]
Secondary outcome measures (1)
- degree of satisfaction with therapy [Time frame: through study completion, an average of 5 years]
Eligibility criteria
Inclusion criteria
- type 2 diabetes mellitus
- presence on the list for OLT for at least 3 months or have already been submitted to OLT for at least 3 months
- age ≥ 18 years
- signature of written informed consent to participate in the observational study, either by the participant or legal guardian
Exclusion criteria
\- Pregnancy or breastfeeding
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Italy · 1 center
- Lucia Brodosi — Bologna
Identifiers
NCT: NCT06816303 · DiaBoLT2021