CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 20 enrolled
Drug / intervention
Furosemide +3 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05779943
NCT05779943Phase 2Active

Strategy to Reduce Bladder Activity With RhPSMA 7.3: Comparison of 18F-RhPSMA 7.3 PET/CT With and Without Furosemide in Biochemical Recurrence of Prostate Cancer

Emory University·interventional·Posted Mar 22, 2023·Updated Oct 27, 2025

In Brief

A Phase 2 clinical trial evaluating Furosemide, F18-rhPSMA-7.3, and 2 other interventions for Prostate Adenocarcinoma and Recurrent Prostate Carcinoma. Active but no longer recruiting, targeting 20 participants across 4 sites.

Detailed Summary

This phase II trial evaluates Fluorine-18 radiohybrid prostate-specific membrane antigen (18F- rhPSMA)-7.3 positron emission tomography (PET)/computed tomography (CT) scans with and without furosemide for the reduction of bladder activity in patients with prostate cancer that has come back (recurrent) based on elevated levels of prostate-specific antigen (PSA) in the blood (biochemical) after prostate surgery (prostatectomy). Furosemide is a diuretic substance that increases the urine flow into the bladder, thereby decreasing the level of radioactivity within the bladder, which may help to see any abnormal areas that could be masked by the radioactivity within the bladder. PET is an established imaging technique that utilizes small amounts of radioactivity attached to very minimal amounts of tracer, in the case of this research, rhPSMA ligand. CT utilizes x-rays that traverse body from the outside. CT images provide an exact outline of organs and potential inflammatory tissue where it occurs in patient's body. Adding furosemide to 18F-rhPSMA 7.3 PET/CT scans may help to better detect and treat patients with biochemically recurrent prostate cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2Active
20242025202620272028
First PostedMar 22, 2023
Enrollment StartApr 27, 2023
Primary CompletionMar 15, 2024
Study CompletionJul 1, 2028
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 3.3 years ago

Interventions

Furosemidedrug

Given IV

F18-rhPSMA-7.3other

Given IV

Positron Emission Tomographyprocedure

Undergo PET/CT scan

Computed Tomographyprocedure

Undergo PET/CT scan