Cleveland, OHNCT05590624Now EnrollingIRB Ready

Prostate Cancer Clinical Trial in Cleveland, OH

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

Sponsored by Case Comprehensive Cancer Center

Quick Self-Assessment

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Expert Care in Cleveland

Access prostate cancer specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related prostate cancer treatment provided free

Apply for This Cleveland Location

Check if you qualify for this prostate cancer clinical trial in Cleveland, OH

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Cleveland

    Convenient for OH 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 Cleveland site if eligible
  4. 4Begin participation

About This Prostate Cancer Study in Cleveland

The purpose of this study is to examine the impact of Mediterranean-type diets on the metabolism of men with localized prostate cancer. The optimal diet for men with a suspected diagnosis of Prostate Cancer (PCa) is currently unknown. More specifically, the suggested benefits of low carbohydrate and low fat diets in PCa are not determined.

Sponsor: Case Comprehensive Cancer Center

Who Can Participate

Inclusion Criteria

Males ≥18 years old
High suspicion of prostate cancer (PCa) per urologist's clinical evaluation
No prior PCa diagnosis or hormonal therapy (-ies)
Ability to read, write, speak, and understand English
Ability to provide informed consent
Candidate for and elects active surveillance (AS) if diagnostic biopsy is positive
Willingness to consume provided dietary interventions
Adequate organ and marrow function: White blood cell count (WBC) ≥2,500/mcL, Absolute neutrophil count (ANC) ≥1,500/mcL, Platelets ≥100,000/mcL, Hemoglobin ≥9 g/dL (transfusions permitted), Total bilirubin ≤1.5 x the institutional upper limit of normal (ULN) (for subjects with Gilbert's disease ≤3.0 mg/dL), Aspartate aminotransferase (AST)/Alanine aminotransferase (ALT) ≤2.5 x institutional ULN, Creatinine clearance ≥51 ml/min as defined by Cockcroft-Gault equation

Exclusion Criteria

Currently consuming a Mediterranean, lower carbohydrate, ketogenic, vegan, vegetarian, high fiber diet (14g fiber \> per 1,000 Calories) and/or any supplements (including herbal), vitamins, minerals, that would interfere with diets being tested in the study as determined by dietitian and/or investigators.
Previous intolerability to fiber-rich diets
Colitis, Irritable Bowel Syndrome, or other gastrointestinal condition per clinician discretion
Unwilling to undergo transperineal PCa biopsies
Food allergies or other major dietary restrictions
Receiving active medical treatment for Type I or Type II diabetes mellitus
Prior antibiotic usage (i.e. within last 30 days) at time of consent
Recent weight loss (both intentional and unintentional) as defined by 5%+ body weight in the last 30 days
Undergone any type of weight loss surgery
Any medical contraindications as determined by investigators
High risk as defined by PSA≥20 and/or PI-RADS 5 lesion as per clinician evaluation
History of diabetic ketoacidosis
Patients that are immunosuppressed (transplant history, on immunosuppression, etc.) as per clinician discretion
Recent (within last 30 days) device implant/joint requiring antibiotics as per clinician determination
Prior history of prostate biopsy infection
Uncontrolled hypertension as defined by blood pressure greater than 140/80 (with or without medication)
Gallbladder removed or plan to remove per clinician evaluation
Other malignancies actively receiving systemic treatment as per clinician evaluation

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 Cleveland?

Yes, this clinical trial (NCT05590624) has an active research site in Cleveland, OH 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 Cancer Treatment Options in Cleveland, OH

If you're searching for prostate cancer treatment options in Cleveland, OH, this clinical trial (NCT05590624) 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 Cleveland research site is actively enrolling participants for this clinical trial. You'll receive care from experienced prostate cancer 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 cancer clinical trials near you to find additional studies recruiting in your area.

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