Monitoring of Treatment Related Toxicities From Oral Targeted Agents and Immunotherapy Among Patients With Advanced Renal Cell Carcinoma (RCC) Using Carevive Software, a Single-Arm Phase II Feasibility Study


Condition: Advanced Renal Cell Carcinoma

Study Type: Interventional

Clinical Trials Identifier NCT 8-digits: NCT03229083

Sponsor: University of Rochester

Eligibility:

  • Age: minimum 18 Years maximum N/A
  • Gender: All

Inclusion Criteria:

  • Diagnosis of histologically confirmed renal cell carcinoma of any subtype with either pathological or radiographic evidence of metastatic disease
  • Greater than 18 years of age
  • A participating Wilmot Cancer Center oncologist has determined that candidate should be started on either oral targeted therapy or immunotherapy for treatment of their advanced RCC; this can be for first-line or any subsequent line therapy
  • Able to provide written informed consent
  • Proficient in the English language and self-reports as literate
  • Must have an active email address or access to a smart device on which text messages can be received

Exclusion Criteria:

  • Women cannot be breast-feeding
  • Does not have regular access to the internet
  • Unable to come to the Wilmot Cancer Center for appointments every 3-4 months for routine visits with their primary oncologist
  • Subjects who were on the study previously will not be allowed to re-enroll in the event of a treatment change

View trial on ClinicalTrials.gov