Actively Recruiting
Adult Patients With Diabetes Mellitus on Drug Treatment on the List or Already Undergoing Orthotopic Liver Transplantation: an Observational Study
Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-02-10
100
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This observational study focuses on adult patients with type 2 diabetes mellitus who are either on the waiting list for orthotopic liver transplantation (OLT) for at least three months or have already undergone OLT for at least three months. The research aims to gather detailed information on metabolic compensation, patient satisfaction with hypoglycemic treatment, the onset of complications related to diabetes or liver disease, and overall survival. It is sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna. Participants are observed without any specific intervention, allowing researchers to monitor their natural health progress and treatment satisfaction. The study will primarily measure glycosylated hemoglobin levels over an average follow-up period of five years. Secondary outcomes include evaluating how satisfied patients are with their therapy during this time. During the study, participants will undergo regular assessments to monitor blood sugar control and report their satisfaction with treatment. Researchers will collect data over about five years to evaluate the long-term metabolic control, complications, and survival rates. No experimental treatments are given, and participants continue their usual medical care throughout the observation period.
CONDITIONS
Brief Title
Patients With Diabetes Mellitus on Drug Treatment on the List or Already Undergoing Orthotopic Liver Transplantation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Type 2 diabetes mellitus
- On the list for orthotopic liver transplantation for at least 3 months or have undergone transplantation at least 3 months ago
- Age 18 years or older
- Signed informed consent by participant or legal guardian
You will not qualify if you...
- Pregnancy or breastfeeding
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 5 years
Participants are observed to monitor glycosylated hemoglobin and satisfaction with therapy over time.
Periodic visits as scheduled by the study team
Trial Site Locations
Total: 1 location
1
Lucia Brodosi
Bologna, BO, Italy, 40138
Actively Recruiting
Research Team
L
Lucia Brodosi
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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