NCT01823562CompletedPhase 1
Aborption and Metabolism of Lyophilized Black Raspberry Food Products in Men With Prostate Cancer Undergoing Surgery
Dietary Fruit Bioactives and Prostate Cancer
Source: ClinicalTrials.gov · Last updated 20 May 2026
Brief summary (registry, in English)
This Phase I/Ib trial is studying the absorption and metabolism of phytochemicals found in black raspberries in men undergoing surgery for prostate cancer. This knowledge will help us design future chemoprevention studies and assist in making future dietary recommendations for men at high risk for prostate cancer.
- Status (registry)
- Completed
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 60 (actual)
- First submitted
- 28 Mar 2013
- Start date
- 17 Oct 2012
- Primary completion date
- 1 Aug 2013
- Lead sponsor
- Ohio State University Comprehensive Cancer Center
- Diseases
- Prostate cancer, Childhood cancers
- NCT number
- NCT01823562
What you commit to
- Study type: Interventional · Phase 1
- Participants enrolled: 60
- From 17 Oct 2012 to the primary completion date, 1 Aug 2013
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Are taking certain medications; no concurrent finasteride (Proscar) or other hormonal agents for chemoprevention/treatment of benign prostate hyperplasia (BPH); utilizing prescription medications for urinary outlet obstructive symptoms will not be permitted; the use of non-prescription substances to improve urinary tract symptoms will not be permitted (i.e. Saw Palmetto, other herbal, alternative products)
- Have significant loss of gastrointestinal organs due to surgery, except for appendix
Other illness
- Have an active malignancy other than prostate cancer that requires therapy
- Have a prostate biopsy with less than 5% cancer involvement
- Have a history of traumatic or surgical castration
- Have a history of pituitary hormone diseases that currently require supplemental hormonal administration (thyroid hormones, adrenocorticotropic hormone \[ACTH\], growth hormone) or other endocrine disorders requiring hormone administration with the exception of diabetes and osteoporosis
- Have a known allergy to black raspberries, corn, and wheat products or those who have never consumed any of these products
- Have active metabolic or digestive illnesses such as malabsorptive disorders (Crohn's, Celiac disease, irritable bowel syndrome \[IBS\]), renal insufficiency, hepatic insufficiency, cachexia, or short bowel syndrome
- Have altered immunity such as autoimmune disorders, cancer, anemia, hemophilia, and blood dyscrasias
- Have noticeable open lesions in the oral cavity, sores that have not healed for more than 2 months or have a history of leukoplakia, tumors of the buccal cavity, throat, and lips
Lab values
- Are taking medications that inhibit clotting (warfarin sodium) or using prescribed oral rinses (Peridex)
Other
- Have difficulty swallowing (dysphagia), pain with swallowing (odynophagia), salivary gland dysfunction, or xerostomia (dry mouth)
Who the study is looking for
- Have biopsy proven carcinoma of the prostate
- Have chosen a radical prostatectomy for treatment of their disease after the medical team has presented all possible treatment options
- Not be receiving neoadjuvant hormonal or chemotherapy (other clinical trials)
- Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
- Not currently taking berry dietary supplements, or "alternative" products (Acai berry, pomegranate, black raspberry, Optiberry, Juice Plus)
- Have BUN/Cr (blood urea nitrogen and serum creatinine) within normal limits
- Have liver enzymes within normal limits
- Have complete blood count (CBC) within normal limits
- Have prothrombin time/partial thromboplastin time (PT/PTT/INR) within normal limits
- Voluntarily agree to participate and sign an informed consent document
- Agree to have prostate biopsy blocks provided to the study for evaluation
- Agree to consume a standardized vitamin and mineral supplement and avoid other nutrition, dietary, or alternative medications/supplements for the duration of the study
- Agree to follow a controlled polyphenolic and/ or ellagitannin diet
Sex: Male · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University Medical Center Coordinator of this site? Confirm its status | Columbus | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.