Diabetes Research Institute
Miami, Florida, 33136, United States
Location status: Recruiting
Location contact
Ana M Alvarez, APRN
CONTACT
David A Baidal, MD
SUB_INVESTIGATOR
Rodolfo Alejandro, MD
CONTACT
Rodolfo Alejandro, MD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT02000687
This is a single-center, prospective, open label study in islet transplant recipients following islet graft loss.
Interested in participating?
Request Info18 year–75 year
All sexes
Observational
Miami, Florida, 33136, United States
Location status: Recruiting
Ana M Alvarez, APRN
CONTACT
David A Baidal, MD
SUB_INVESTIGATOR
Rodolfo Alejandro, MD
CONTACT
Rodolfo Alejandro, MD
PRINCIPAL_INVESTIGATOR
After complete islet graft loss is determined, patient's maintenance immunosuppression (i.e. sirolimus, tacrolimus, MMF and/or Myfortic®) will be discontinued and they will be monitored for 10 years thereafter, for the appearance of allosensitization using panel reactive antibody (PRA) levels and monitor the persistence of elevated PRA levels. Primary objective is to determine the rate of allosensitization in patients 3 years after failed islet transplantation (i.e. stimulated c-peptide <0.3mg/mL) and monitor the persistence of elevated PRA levels (≥ 20%) at year 3, 6, and 9. Timing, frequency and level of change in PRA will be monitored after all immunosuppression is discontinued.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 10 years
Rodolfo Alejandro
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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