Actively Recruiting

Age: 18Years +
All Genders
ID06816303

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • Pregnancy or breastfeeding

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

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

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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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