🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in the USA / NCT07564102
Starting soon Phase 1/2

dMD-002 Pilot Study in Patients With Cavernous Nerve Injury Following Radical Prostatectomy

NCT07564102 · tracked via the Priya Life Science USA tracker
Sponsor
Mochida Medical USA, Inc.
Phase
Phase 1/2
Started
2026-08-01
Last updated
2026-05-15

Condition(s) studied

Prostate Cancer

Investigational drug(s) / intervention(s)

dMD-002Control

dMD-002: The cut dMD-002 is implanted to cover the nerve injury, tear, or defect, and is fixed by suturing to the surrounding tissue in two or more places.

Control: Prostatectomy without dMD-002

Study summary

The purpose of this study is to conduct a US Pilot study of dMD-002 as a peripheral nerve repair sheet in patients with cavernous nerve injury following radical prostatectomy. The study will determine which endpoints and timepoints will be used for the pivotal study.

Eligibility

Sex
MALE
Min age
40 Years
Max age
74 Years
Healthy volunteers
No
Inclusion Criteria: * Patients diagnosed with prostate cancer. * Patients scheduled to undergo a robot-assisted radical prostatectomy (including either bilateral-nerve sparing or unilateral-nerve sparing) for treatment of prostate cancer. etc. Exclusion Criteria: * Patients undergoing pre-surgery or post-surgery radiation therapy, hormone therapy, or anti-cancer therapy. * Patients who have used a penile prosthesis implantation. * Patients with a history of transurethral resection, laser therapy, microwave therapy, radiofrequency ablation, cryoablation, or other prostate surgery. etc.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Icahn School of Medicine at Mount Sinai New York New York

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07564102 on ClinicalTrials.gov ↗ ← All trials in the USA