RecruitingACTRN12618000627257

National Dermatology Radiation Oncology Registry: A multi-site Registry recording clinical observations of patients referred for radiotherapy for the management of skin cancers and inflammatory skin diseases


Sponsor

Genesis Cancer Care and Specialist Connect Services

Enrollment

10,000 participants

Start Date

May 17, 2018

Study Type

Observational

Conditions

Summary

The National Dermatology Radiation Oncology Registry (NDROR) is a human research Registry that collects and collates information from patients referred for radiotherapy for the management of non-melanoma and melanoma skin cancer and difficult to manage inflammatory skin diseases. Who is it for? Patients aged 18 years or above will be recruited based on referral from their current treating dermatologist to a Genesis Cancer Care (GCC) Radiation Oncologist once diagnosed with a lesion or condition deemed treatable with radiotherapy. Study details Data may be collected from eligible patients retrospectively regarding their previous relevant medical history, and prospectively, including treatment schedule and treatment outcomes of their radiotherapy treatment. Upon agreeing to participate in the NDROR, the referring dermatologist (RD) will send information to the Treating Radiation Oncologist (TRO). Previous relevant medical history as well as current treatment plans will be imported by both RD and TROs into the data Registry called the Skin and Radiotherapy Online Secure Platform (OSP). The intended outcome of this Registry is to ultimately assess the safety, tolerability and outcomes of treatment. Although treatment of skin cancer and inflammatory skin conditions with radiotherapy is currently used, limited practical evidence into the safety, tolerability and outcomes based evidence has been established in Australia. This Registry will be the first of its kind in Australia and will provide a basis for a number of research publications assessing these outcomes.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Inclusion Criteria4

  • over 18 years of age
  • diagnosed with a treatable skin cancer or inflammatory skin condition by a dermatologist
  • elligible to be treated using radiotherapy
  • patient has voluntarily signed and dated informed consent/patient authorisation form

Exclusion Criteria1

  • patients who do not consent to their involvement in the registry

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Interventions

The Registry is a human research registry that collects and collate information from patients referred for radiotherapy for the management of melanoma, and non melanoma skin cancers and difficult to m

The Registry is a human research registry that collects and collate information from patients referred for radiotherapy for the management of melanoma, and non melanoma skin cancers and difficult to manage inflammatory skin diseases. Non-interventionalist observations of radiotherapy treatment for skin cancer and other inflammatory skin conditions for patients referred by a Dermatologist. The Registry will be recording demographics, relevant medical history, lesion assessment, treatment outcomes and follow up. Participant follow up is as follows: - Immediately after and 3 months post treatment with Treating Radiation Oncologist = 6, 12, 18, 24 months post treatment and yearly there after with Referring dermatologist as per their usual standard of care. There is an option to record data post the two year period if as part of usual routine of care. This Registry data will be used in future studies to prospectively assess treatment outcomes for patients undergoing radiotherapy for skin their skin.


Locations(1)

ACT,NSW,NT,QLD,SA,TAS,WA,VIC, Australia

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ACTRN12618000627257