A multi-center randomized blinded controlled study to evaluate the safety and efficacy of the Urocross Expander System and Retrieval System (EXPANDER-2)

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    Benign Prostate Hyperplasia
  • Age: Between 45 Year(s) - 100 Year(s)
  • Gender: Male
  • Other Inclusion Criteria:
    1. Subject has signed an informed consent form (ICF)
    2. Men = 45 years
    3. Subjects willing to be off their BPH-related medications from time of enrollment and throughout the study

    4. Note: All subjects on BPH-related m

You may not be eligible for this study if the following are true:

    1. Previous BPH procedure intended to disobstruct the bladder outlet (e.g., prostate surgery, stent implantations, laser prostatectomy, hyperthermia or another invasive treatment to the prostate).
    2. Biopsy of the prostate within past 8 week

If you are registered as a volunteer, please log in to contact the study team/express interest in this study.

Contact the research team to learn more about this study.

By clicking "Contact Research Team", your contact information will be sent securely to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.