Orange, CANCT06446648Now EnrollingIRB Ready

Prostate Adenocarcinoma Clinical Trial in Orange, CA

Access cutting-edge prostate adenocarcinoma treatment through this clinical trial at a research site in Orange. Study-provided care at no cost to qualified participants.

Sponsored by University of California, Irvine

Quick Self-Assessment

See if you qualify for this Orange location

Preparing your pre-screening questions…

Expert Care in Orange

Access prostate adenocarcinoma specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related prostate adenocarcinoma treatment provided free

Apply for This Orange Location

Check if you qualify for this prostate adenocarcinoma clinical trial in Orange, CA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Orange

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Orange site if eligible
  4. 4Begin participation

About This Prostate Adenocarcinoma Study in Orange

This is a pilot, 3 phases open-label feasibility study with the 3rd phase consisting of randomized 2-arm intervention trial, to assess the systematic use of indocyanine green (ICG) in subjects with prostate adenocarcinoma during robot-assisted radical prostatectomy and its impact on sexual function outcomes at 12 months postoperatively.

Sponsor: University of California, Irvine

Who Can Participate

Inclusion Criteria

1\. Subjects must be ≥18 years old and male.
2\. Histologically/pathologically confirmed localized prostate adenocarcinoma.
3\. Most recent preoperative Sexual Health Inventory for Men (SHIM) score ≥10.
4\. Subjects who are candidates for good nerve sparing preoperatively determined by the investigator by assessing imaging findings.
5\. Ability to read, write and understand and willingness to sign a written informed consent.
6\. Subjects must pass medical clearance from primary care provider and cardiologist, if applicable.
7\. Subject must be determined to be medical fit for RARP by the investigator.

Exclusion Criteria

1\. No locally advanced or metastatic prostate adenocarcinoma.
2\. Preoperative diagnosis of erectile dysfunction with any use of invasive interventions such as intrapenile injections and intrapenile prosthesis implants. Oral interventions are acceptable and are not exclusionary.
3\. Received neoadjuvant treatment for high-risk prostate cancer or received prior focal treatment of the prostate or prior definitive radiotherapy.
4\. History of allergic reactions or hypersensitivity attributed to iodide compounds, ICG, or any component of ICG.
5\. Subjects who are preoperatively not foreseen as ideal candidates for nerve sparing interventions by the investigator.
6\. Subjects who are unable to comply with study and follow-up procedures as judged by the investigator.
7\. Subjects who are illiterate.
8\. Other serious, uncontrolled concomitant diseases that may affect protocol compliance or interpretation of outcomes, including active opportunistic infections or advanced (severe) infections, or uncontrolled diabetes.
9\. Any other disease, metabolic disorder, or abnormal finding upon physical examination or laboratory examination that makes the subject unsuitable for receiving the intervention, affects the interpretation of study outcomes, or poses risks to subject safety, as determined by the investigator.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Orange?

Yes, this clinical trial (NCT06446648) has an active research site in Orange, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Prostate Adenocarcinoma Treatment Options in Orange, CA

If you're searching for prostate adenocarcinoma treatment options in Orange, CA, this clinical trial (NCT06446648) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Orange research site is actively enrolling participants for this clinical trial. You'll receive care from experienced prostate adenocarcinoma specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all prostate adenocarcinoma clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Orange, CA