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Recruiting NCT07567027

Improving Cryoablation Efficacy With BARRigel Rectal Spacing (ICE-BARR)

Conditions: Prostate Cancer (Diagnosis), Transperineal Cryoablation

Sex: Male
Ages: 40 Years – 95 Years
Healthy volunteers: No
Phase: NA
Enrollment: 20
Sponsor: NYU Langone Health

Location: NYU Langone Health New York New York

Summary

The purpose of this study is to evaluate the feasibility, safety, and potential protective benefit of Barrigel, a hyaluronic acid-based rectal spacer, in patients undergoing prostate cryoablation for localized or recurrent prostate cancer. The primary aim is to assess Barrigel thermal stability during cryoablation.

Eligibility Criteria

Inclusion Criteria: * Male patients aged 40-95 years. * Biopsy-confirmed localized prostate cancer (Grade Group ≥ 2). Salvage cryoablation cases may be included. * Unifocal disease visible on multiparametric MRI (mpMRI) and amenable to focal or whole gland cryoablation. * Prostate-specific antigen (PSA) \< 20 ng/ml. * No metastatic disease on Prostate-Specific Membrane Antigen (PSMA) PET/CT, when recommended per National Comprehensive Cancer Network (NCCN) guidelines. * Eligible for and consenting to transperineal cryoablation under anesthesia. * Willingness to comply with post-procedure follow-up, including PSA testing and imaging. * Cryoablation which requires treatment of the posterior prostate as per clinician judgement. Exclusion Criteria: * Evidence of metastatic disease. * Prior radiation therapy to the area of the prostate. * Active rectal or urinary tract infection. * Known allergy to hyaluronic acid products or contrast agents. * Inability to tolerate MRI. * Inability or unwillingness to comply with study follow-up.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07567027). StuddyBuddy aggregates publicly available trial information.