About this trial

The objective of this study is to compare a new surgical technique for HoLEP that will allow for sparing of ejaculation post-HoLEP.

Eligibility criteria

Qualifiers

None

Disqualifiers

Patients with pre-existing retrograde ejaculation

Patients who are not sexually active

Patients with indwelling urinary catheter prior to surgery, neurological disease, or history of prior prostatic/urethral surgery that may impact ejaculation

Patients who lack decisional capacity

Trial design

Treatments tested in this trial

  • Ejaculatory-sparing (ES-sparing) HoLEP

Treatment groups

48 Participants
are divided into 2 treatment groups

Locations

1
Northwestern University60611, ChicagoIllinois, United States

Sponsors and collaborators

Northwestern University

Lead sponsor