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New treatment option for Prostate Adenocarcinoma
Official title The Use of Ultrasound in Assessing Post-prostatectomy Erectile Dysfunction
ClinicalTrials.gov ID: NCT05109208
What this study is testing
- What it's testing
- Researchers are trying to determine whether there is additional utility to using vibroelastography, a noninvasive ultrasound technique to evaluate for the presence of tissue fibrosis, in conjunction with standard penile duplex Doppler ultrasound to assess erectile function (recovery) after prostate cancer surgery.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 40 and older, men only
You may be able to join if
- include:
- Age \> 40 years
- Clinically localized prostate cancer (American Urological Association Grade Groups 1-2; cT1c or cT2a-b; PSA \< 10) without clinic or imaging evidence...
- International Index of Erectile Function (IIEF) of ≥ 21 points at baseline (no or mild erectile dysfunction)
- Patient-expressed interest in consultation for sexual function (erectile function) preservation/ optimization
You likely can't join if
- include:
- Moderate or severe ED based in IIEF criteria (score \< 21)
- History of prior pelvic or penile surgery
- Current or prior androgen deprivation therapy
- Planned non-nerve sparing prostatectomy
See the full eligibility criteria
- include:
- Age \> 40 years
- Clinically localized prostate cancer (American Urological Association Grade Groups 1-2; cT1c or cT2a-b; PSA \< 10) without clinic or imaging evidence of localized extra-prostatic or metastatic disease (i.e. AUA low and...
- International Index of Erectile Function (IIEF) of ≥ 21 points at baseline (no or mild erectile dysfunction)
- Patient-expressed interest in consultation for sexual function (erectile function) preservation/ optimization
- Planned bilateral nerves-paring prostatectomy
- include:
- Moderate or severe ED based in IIEF criteria (score \< 21)
- History of prior pelvic or penile surgery
- Current or prior androgen deprivation therapy
- Planned non-nerve sparing prostatectomy
The study team makes the final eligibility decision.
Where it's taking place
- Rochester, Minnesota, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling male, 40 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Rochester, Minnesota, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.