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Prostate Cancer clinical trials

View clinical trials related to Prostate Cancer.

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NCT ID: NCT02091661 Suspended - Prostate Cancer Clinical Trials

Radical Retropubic Prostatectomy Versus Conventional External Beam Radiotherapy for Clinically Localized Prostate Cancer

Start date: January 1997
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of the two most established primary treatments for patients with clinically localized prostate cancer: radical retropubic prostatectomy, and external-beam radiotherapy. The primary aim is assessing biochemical disease-free survival, overall survival, and prostate cancer-specific survival. As secondary objectives quality of Life impact of treatments' side effects will be also assessed.

NCT ID: NCT02090114 Completed - Prostate Cancer Clinical Trials

RE-sensitizing With Supraphysiologic Testosterone to Overcome REsistance (The RESTORE Study)

Restore
Start date: August 25, 2014
Phase: Phase 2
Study type: Interventional

Single-arm, single site, open label study of the effects of parenteral testosterone followed by enzalutamide, abiraterone or castration-only therapy in men with metastatic CRPC who previously progressed on one of these forms of therapy. The study will enroll four cohorts of patients: men with metastatic CRPC who have progressed on enzalutamide (Cohort A; n=30); men with metastatic CRPC who have progressed on abiraterone acetate (Cohort B; n=30); men with metastatic CRPC who have progressed on first line castration-only therapy (Cohort C; n=30); men with metastatic CRPC with inactivating somatic or germline mutations in ≥2 of the genes TP53, PTEN, or RB1 (Cohort D; n=20).

NCT ID: NCT02088164 Completed - Prostate Cancer Clinical Trials

Long-Term Outcome of Subjects With Elevated PSA in Healthy Taiwanese Men

Start date: February 2012
Phase: N/A
Study type: Observational

To determine the long-term survival outcome of subjects who had various PSA levels at screening

NCT ID: NCT02086266 Completed - Prostate Cancer Clinical Trials

The Efficacy of Pilates in the Recovery of Post-prostatectomy Urinary Incontinence

Start date: March 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficacy between a Pilates exercise program and a Pelvic Floor Muscle Training (PFMT) protocol combined with anal electrical stimulation (AES) in the recovery of urinary continence (UI) after radical prostatectomy. There are no studies that evaluate Pilates mat exercises for incontinence in men although it can be assured that this method has the pelvic floor contractions as a principle for practice. If this new therapeutic approach proves to be as effective as described treatment in improving urinary complaints, it will be an option for patients who prefer a non-invasive treatment.

NCT ID: NCT02085252 Completed - Prostate Cancer Clinical Trials

A Study of the Effect of Enantone LP 11.25 mg (Leuprorelin) on the Histological Progression of Indolent Prostate Cancer

Start date: June 3, 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess two treatment strategies (leuprorelin treatment and active surveillance without androgen deprivation) for indolent prostate cancer and to compare their therapeutic benefit for management of patients with low-risk, localized prostate cancer.

NCT ID: NCT02085096 Completed - Prostate Cancer Clinical Trials

Problem Solving Therapy for Prostate Cancer Spousal Caregivers

Start date: July 1997
Phase: N/A
Study type: Interventional

Problem-solving therapy programs have been shown to be effective among parents of children diagnosed with cancer. Efforts have been made to apply this same strategy to spouses/significant others of men diagnosed with prostate cancer. The purpose of this study is to test the efficacy of problem-solving therapy on the spouses of prostate cancer patients.

NCT ID: NCT02083185 Completed - Prostate Cancer Clinical Trials

A Phase 2 Study to Evaluate the Safety and Efficacy of TAK-385, Together With a Leuprorelin Observational Cohort, in Participants With Prostate Cancer

Start date: March 26, 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of TAK 385 for achieving and maintaining testosterone suppression (<50 ng/dL).

NCT ID: NCT02080689 Completed - Prostate Cancer Clinical Trials

Prospective Clinical Utility Study to Assess the Impact of Decipher on Treatment Decisions After Surgery

PRO-IMPACT
Start date: May 2014
Phase: N/A
Study type: Interventional

The influence of Decipher test on urologist and patient treatment plan choices immediately post RP and at the time of PSA rise or BCR

NCT ID: NCT02080650 Completed - Prostate Cancer Clinical Trials

Characterization of Circulating Tumor Cells Captured by c-MET (CTC-MET)

Start date: March 2014
Phase: N/A
Study type: Interventional

This pilot study will aim to determine whether circulating tumor cells (CTCs) can be captured using the novel cMET based ferrofluid. The primary objective of this pilot study will be to describe the numbers of c-MET expressing cells that can be detected by the c-MET CTC capture technique. These data will be separated by disease site. The investigator will also describe the detection rates of both the c-MET CTC capture and the EpCAM CTC capture techniques in each patient, also separated by disease site.

NCT ID: NCT02080052 Completed - Prostate Cancer Clinical Trials

Robot-Assisted MRI-Guided Prostate Biopsy

Start date: July 25, 2013
Phase: N/A
Study type: Interventional

Prostate biopsies are commonly performed freehanded under transrectal ultrasound guidance (TRUS). Due to the manual approach and the limitations of the ultrasound imager, the procedure has high false-negative rates. This represents a daily problem for urologists managing the disease, creates uncertainty and emotional stress for patients, and initiates a cascade of repeat testing and biopsies which also burden the investigators healthcare system. The investigators believe that prostate biopsy can be improved by using a new biopsy paradigm. The investigators plan to perform MRI-guided prostate biopsies with robot-assistance for orienting a needle-guide through which the biopsy is taken. The combination of MRI and robotic precision is expected to improve prostate biopsy sensitivity compared to regular TRUS biopsies. The study is a Pilot clinical trial on 5 patients to primarily assess feasibility and safety. The needle-guide robot is an investigational device developed in their Urology Robotics Laboratory.