Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
4000 participants
OBSERVATIONAL
2008-01-31
2019-12-31
Brief Summary
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Detailed Description
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This study is a prospective observational cohort study of kidney, heart, lung, liver, pancreas and small bowel transplant recipients enrolled into the Swiss Transplant Cohort Study (STCS).
Since 2008 almost all organ transplant recipients in Switzerland are enrolled to the STCS. The STCS collects
* baseline patient and case data: date of transplantation, age, gender, type of transplanted organ, past immunosuppression
* follow-up patient and case data: organ rejection with type and date of rejection, type of immunosuppression in response to organ rejection, graft loss with date of graft loss, immunosuppressive drug treatment, other drug treatment, death, drop out, occurrence of cancer and infections)
* drug exposure data (with start and stop dates): induction immunosuppressive drugs (Basiliximab, Rituximab, Thymoglobulin, ATG, ATGAM, IG iv, Plasmapheresis), maintenance immunosuppressive drugs (Cyclosporine A, Glucocorticoids, Tacrolimus, Mycophenolate mofetil, Everolimus, Azathioprine, Sirolimus, EC-MPA), infectious disease prophylaxis (e.g. TM-Sulfamethoxazole, Valaciclovir, Fluconazole, Atovaquone, Voriconazole, Quinolone), other drugs (e.g. Statins, beta-Blockers, oral antidiabetics).
The investigators will statistically illustrate the incidence, prevalence and type of skin neoplasms in the STCS. The investigators will show the association of the incidence of skin neoplasms and the exposure to different immunosuppressive drugs, other drugs and other parameters in the STCS (e.g. age, gender).
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* patients with multiple organ transplantations will be included as well
* patients within the STCS, who gave the informed consent to use their data
* patients with graft loss will remain in the study, since they remain at risk of skin cancer development
Exclusion Criteria
1 Hour
ALL
No
Sponsors
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University of Zurich
OTHER
Responsible Party
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Principal Investigators
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Günther Hofbauer, Prof MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital Zurich, Dermatology
Locations
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University Hospital Zurich, Dermatology
Zurich, , Switzerland
Countries
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Other Identifiers
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KEK-ZH-Nr. 2014-0276
Identifier Type: -
Identifier Source: org_study_id
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