Kidney Cancer Clinical Trial
Investigation of Cisplatin-Related Kidney Toxicity
Summary
The purpose of this study is to identify novel biomarkers of kidney injury in patients receiving cisplatin.
This study will also collect DNA for future analysis.
Full Description
This study will look for novel biomarkers of kidney injury in patients receiving cisplatin in patients currently receiving cisplatin.
DNA will be collected both prospectively and retrospectively (from patients that have previously received cisplatin.
Eligibility Criteria
Prospective Analysis Group
Inclusion Criteria:
Patients about to receive intravenous cisplatin for the first time as part of cancer chemotherapy.
Aged 18 years and older.
Ability to understand and willingness to sign a written consent document.
Patients may be receiving cisplatin in combination with other chemotherapeutic agents.
Patients may be receiving cisplatin in the context of another clinical trial.
Exclusion Criteria:
Prior receipt of cisplatin.
Patients on dialysis or other renal replacement therapy prior to starting cisplatin.
Uncontrolled hypo- or hyperthyroidism (patients on chronic stable doses of thyroid replacement medication are eligible).
Retrospective Analysis Group
Inclusion Criteria:
Patients that have previously received intravenous cisplatin as part of cancer chemotherapy.
Aged 18 years and older.
Ability to understand and willingness to sign a written consent document.
Patients that received cisplatin in combination with other chemotherapeutic agents are eligible.
Patients that received cisplatin in the context of a clinical trial are eligible.
Exclusion Criteria:
Unable or unwilling to submit to a one-time blood draw.
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There is 1 Location for this study
Chicago Illinois, 60637, United States
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