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NCT06458855Active, not recruiting

Nerve Grafting Technique to Restore Erectile Function Post Radical Prostatectomy

Pilot Trial: Pilot Study of Somatic-Autonomic Nerve Grafting Technique to Restore Erectile Function in Patients With Persistent Erectile Dysfunction Post Radical Prostatectomy

Source: ClinicalTrials.gov · Last updated 18 Apr 2025

Brief summary (registry, in English)

A single arm prospective pilot trial evaluating the safety and the 1-year erectile recovery outcomes of patients undergoing a somatic to autonomic nerve grafting procedure for restoration of erectile function in patients who have lost erectile function following radical prostatectomy for prostate cancer. During this study a total of 10 patients who have persistent erectile dysfunction for more than 18 months post prostatectomy will undergo a post radical prostatectomy nerve restoration procedure (PRP-NR).

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
21 May 2024
Start date
17 Jul 2024
Primary completion date
Mar 2027
Lead sponsor
Sir Mortimer B. Davis - Jewish General Hospital
NCT number
NCT06458855

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 17 Jul 2024 to the primary completion date, Mar 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients with previous pelvic radiotherapy

Other illness

  • Patients with pre-existing neurologic disease
  • Patients with a history of bilateral surgeries for inguinal hernia repair.

Age

  • Patients aged \< 18 years at diagnosis

Other

  • Legally incapable patients
  • Patients who are unable to complete questionnaires and have no companion to help complete them

Who the study is looking for

  • Patients with persistent post prostatectomy erectile dysfunction more than 18 months from prostatectomy and which results in the inability to achieve intercourse with the aid of PDE5-I medications.
  • Patients must have had good pre-prostatectomy erectile function with a baseline IIEF score of ≥17 on self-reported assessment of historic function.

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Jewish General Hospital
Coordinator of this site? Confirm its status
MontrealCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.