RT-310 Dose Escalation BPH Study

Status Recruiting

Clinical Trial Summary

RT-310, a novel implant, is intended to minimally invasive treat locally the prostate gland for the management of prostate disease, while minimizing side-effects. The objectives of the study are to assess whether RT-310 is safe and feasible for the participant population.

Clinical Trial Description

The RT-310 study is a first in human Phase 1 multi-center prospective, non-randomized dose escalation study to evaluate the safety and feasibility of RT-310 for treatment of Benign Prostatic Hyperplasia (BPH). Study participants will have placement of RT-310 and be followed through 180 days. ;

Study Design

Related Conditions & MeSH terms

BPH (Benign Prostatic Hyperplasia)
Hyperplasia
Lower Urinary Tract Symptoms
Prostatic Hyperplasia

Clinical Trial Details

NCT number	NCT06136819
Study type	Interventional
Source	Resurge Therapeutics Inc.
Contact
Status	Recruiting
Phase	Phase 1
Start date	February 2024
Completion date	February 2024

View Details

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