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Recruiting

NCT Number: NCT02000687

Long Term Surveillance of Islet Transplant Recipients Following Complete Graft Loss

This is a single-center, prospective, open label study in islet transplant recipients following islet graft loss.

Recruiting

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Diabetes Research Institute

Miami, Florida, 33136, United States

Location status: Recruiting

Location contact

Ana M Alvarez, APRN

CONTACT

[email protected]

305 243-3389

David A Baidal, MD

SUB_INVESTIGATOR

Rodolfo Alejandro, MD

CONTACT

[email protected]

305-243-5321

Rodolfo Alejandro, MD

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • History of at least one islet alone transplant (ie islet transplant in the absence of any other organ transplant).

Exclusion criteria

  • Inability to provide written informed consent.
  • Mentally unstable and/or unable to comply with the procedures of the study protocol.
  • History of any solid organ transplant.

Treatment and study plan

Primary outcomes

  1. determine the rate of allosensitization in patients after failed islet transplantation

    Time frame: 10 years

Sponsors and collaborators

Lead sponsor

Rodolfo Alejandro

Other

Registry information

Important dates

Study start
2008
Primary completion
2027
Study completion
2028
First posted
Dec 4, 2013
Registry last updated
Mar 23, 2026

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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