A Prospective Diagnostic Cohort Study to Compare the Accuracy of Renal Mass Biopsy, PEER, and 99mTc-sestamibi SPECT/CT for Patients With Clinically Localized Renal Tumors

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The goal of this clinical trial is to better tell apart whether kidney tumors are benign (not cancer) or malignant (cancer) based on a biopsy or imaging tests and ask patients how they feel about decisions they make about treatment of their kidney tumor. The main objectives are: To estimate and compare the diagnostic accuracy of renal mass biopsy alone, PEER (with renal mass biopsy), and 99mTc-sestamibi SPECT/CT (with renal mass biopsy for hot tumors) to differentiate malignant and benign renal tumors. To estimate and compare the diagnostic accuracy of renal mass biopsy, PEER (with renal mass biopsy), and 99mTc-sestamibi SPECT/CT (with renal mass biopsy for hot tumors) to differentiate oncocytoma from chromophobe RCC. Participants will be asked to complete survey questions related to their health and kidney tumor at the start and end of the study. These can be done on paper, electronically, or by telephone.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Participants diagnosed with a clinically localized (cT1) renal tumor ≤7cm in size with a solid component suspicious for malignancy based on cross-sectional imaging

• Pre-existing CT images of the mass with and without contrast or planned CT to ensure both with and without contrast images of the mass have been obtained within a 365-day window

• Participants must be greater than or equal to 18 years of age

• Eligible or planned to undergo partial or radical nephrectomy as determined by primary urologist

• Eligible or planned to receive renal mass biopsy as determined by primary urologist

• Estimated glomerular filtration rate of ≥30 ml/min/1.73 m2 as calculated by the CKD-EPI (Chronic Kidney Disease-Epidemiology Collaboration) Equation

Locations
United States
Illinois
Loyola University Medical Center
RECRUITING
Maywood
Contact Information
Primary
Gopal N Gupta, MD
gogupta@lumc.edu
708-216-8467
Backup
Agnes Natonton
anatont@luc.edu
708-327-3295
Time Frame
Start Date: 2023-02-01
Estimated Completion Date: 2033-12
Participants
Target number of participants: 100
Sponsors
Leads: Loyola University

This content was sourced from clinicaltrials.gov

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