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Completed

NCT Number: NCT02751151

Photodynamic Therapy for Prevention of Nonmelanoma Skin Cancer in Organ Transplant Recipients

The study will draw patients from the Transplant Dermatology specialty clinic, where the investigators see organ transplant recipients (OTR) for regular screening and serve as a regional referral center for this population. Enrollment will be limited to 20 patients. Inclusion criteria are organ transplant recipients status, active immunosuppression for at least 5 years, and history of at least one NMSC.

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Inova Melanoma Na Skin Oncology Center

Fairfax, Virginia, 22031, United States

About this study

Patients will receive Levulan Kerastick (aminolevulinic acid) to the face and/or scalp (if both are needed, treated separately on back to back days); incubation: 2.5 hours and blue light photodynamic therapy utilizing the DUSA BLU-U device; illumination: 1000 seconds (16 min, 40 secs); administered quarterly for 3 years. Patients who change systemic immunosuppression regimens or add or increase systemic chemoprevention while in the study will be excluded from the overall analysis. The patients will be evaluated by the principal investigator every 3 months, prior to photodynamic therapy (PDT) administration.

Primary endpoints include:

  • development of non melanoma skin cancers (NMSC) lesions and
  • assessment of actinic damage score.

The primary endpoint will be development of new skin cancers at 3 years, based on comparison to rate at baseline from previous (x) year(s) using absolute slope value for number prior to treatment vs. number after treatment. The patients will serve as their own controls and the investigators will analyze the delta in development of non melanoma skin cancers and actinic damage score pre- and post- treatment.

Additionally, an actinic damage score will be assigned based on the number of actinic keratosis on initial evaluation. At each 3 month follow up visit, the actinic damage score will be reassessed. The investigators will be able to secondarily analyze the delta in the actinic damage score on treatment.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • The patient has been the recipient of any solid organ transplant.
  • Active immunosuppression for at least 5 years
  • History of at least one NMSC
  • Subject is willing to sign an informed consent to participate in this study.

Exclusion criteria

  • Patient is not appropriate candidate for treatment or research trial per treating physician
  • Patient has a mental health condition that makes them unable to participate in this research trial, per PI judgment.
  • Patient is on additional immunosuppression for diagnosis unrelated to organ transplant -

Treatment and study plan

have Levulan Kerastick (aminolevulinic acid) solution

Other

Levulan Kerastick (aminolevulinic acid) solution applied to the face and/or scalp (if both are needed, treated separately on back to back days); with an incubation period of 2.5 hours. Blue light photodynamic therapy utilizing the DUSA BLU-U device, illumination: 1000 seconds (16 min, 40 secs), will be administered

Primary outcomes

  1. Number of non melanoma skin cancers in organ transplant recipients

    Time frame: through study completion, an average of 2 years

Secondary outcomes

  1. Reduction of actinic keratosis damage/epidermal dysplasia in organ transplant recipients as assessed by physician and graded per actinic damage scale

    Time frame: through study completion, an average of 2 years

Sponsors and collaborators

Lead sponsor

Inova Health Care Services

Other

Collaborators

  • DUSA Pharmaceuticals, Inc.

Registry information

Acronym: PDT

Important dates

Study start
2016
Primary completion
2021
Study completion
2021
First posted
Apr 26, 2016
Registry last updated
Oct 6, 2021

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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