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Prostate Adenocarcinoma clinical trials

View clinical trials related to Prostate Adenocarcinoma.

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NCT ID: NCT03996993 Recruiting - Prostate Cancer Clinical Trials

Defining Recurrent Disease With Axumin™

Start date: July 1, 2019
Phase:
Study type: Observational

This project seeks to use advanced imaging (specifically, positron emission tomography/computed tomography [PET/CT]) to detect, locate, and characterize recurrent disease in the setting of patients with prostate cancer.

NCT ID: NCT03982173 Withdrawn - Clinical trials for Metastatic Colorectal Cancer

Basket Trial for Combination Therapy With Durvalumab (Anti-PDL1) (MEDI4736) and Tremelimumab (Anti-CTLA4) in Patients With Metastatic Solid Tumors

MATILDA
Start date: September 2020
Phase: Phase 2
Study type: Interventional

To determine the efficacy (as measured by overall tumour response rate) of the combination of durvalumab and tremelimumab when given to previously treated patients with solid tumors harboring a high mutational load.

NCT ID: NCT03963739 Active, not recruiting - Clinical trials for Prostate Adenocarcinoma

Effect of Treatment on Work Experience in Patients With Stage I-III Prostate Cancer

PCW
Start date: July 19, 2019
Phase:
Study type: Observational

The objective of this study is to examine how adenocarcinoma of the prostate treatment differentially affects African American men's ability to work and to describe and compare changes in work ability (as measured through self-reported global work ability item) reported by African American and white adenocarcinoma of the prostate survivors before treatment and 6 months after treatment completion.

NCT ID: NCT03933670 Recruiting - Prostate Cancer Clinical Trials

Hyperpolarized Pyruvate (13C) MR Imaging in Monitoring Patients With Prostate Cancer on Active Surveillance

Start date: July 18, 2018
Phase: Phase 2
Study type: Interventional

This phase II trial studies the side how well hyperpolarized carbon C 13 pyruvate (HP C-13 pyruvate) magnetic resonance imaging (MRI) works in monitoring patients with prostate cancer on active surveillance who have not received treatment. Diagnostic procedures, such as MRI, may help visualize HP C-13 pyruvate uptake and breakdown in tumor cells.

NCT ID: NCT03899987 Suspended - Clinical trials for Prostate Adenocarcinoma

Aspirin and Rintatolimod With or Without Interferon-alpha 2b in Treating Patients With Prostate Cancer Before Surgery

Start date: November 29, 2019
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well aspirin and rintatolimod with or without interferon-alpha 2b work in treating patients with prostate cancer before surgery. Aspirin may help to keep the prostate cancer from coming back. Rintatolimod may stimulate the immune system and interfere with the ability of tumor cells to grow and spread. Interferon-alpha 2b may improve the body's natural response to infections and may slow tumor growth. It is not yet known how well rintatolimod, aspirin, and interferon-alpha 2b work in treating patients with prostate cancer undergoing surgery.

NCT ID: NCT03880422 Recruiting - Obesity Clinical Trials

Nutrition and Exercise Interventions in Reducing Androgen Deprivation Therapy-Induced Obese Frailty in Prostate Cancer Survivors

Start date: May 2, 2019
Phase: N/A
Study type: Interventional

This trial studies how well nutrition and exercise interventions work in reducing androgen deprivation therapy-induced obese frailty in prostate cancer survivors. Individualized nutrition and exercise advice for prostate cancer patients on androgen deprivation therapy may help to reduce obese frailty and change the levels of myokines in blood.

NCT ID: NCT03860961 Active, not recruiting - Clinical trials for Prostate Adenocarcinoma

Increasing the Dose of Survivorship Care Planning in Improving Care and Outcomes in Prostate Cancer Survivors Receiving Androgen Deprivation Therapy

Start date: August 2, 2019
Phase: N/A
Study type: Interventional

This trial studies how well increasing the dose of survivorship care planning improves care and outcomes in prostate cancer survivors receiving radiation therapy and androgen deprivation therapy. There is a need for coordinated care between the cancer care team with the primary care team. This is especially important for prostate cancer survivors who need routine cancer care follow-up with their radiation oncologist and also coordinated routine follow-up with their primary care provider (PCP). This is important because androgen deprivation therapy increases a patient's risk for developing diabetes, hypercholesterolemia, and cardiovascular events. Increasing the dose of survivorship may improve care and outcomes of cancer survivors than standard practices.

NCT ID: NCT03830164 Completed - Clinical trials for Prostate Adenocarcinoma

Pentoxifylline, Atorvastatin, and Vitamin E in Treating Patients With Erectile Dysfunction After Radiation Therapy for Prostate Cancer

Start date: November 20, 2019
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well pentoxifylline, atorvastatin, and vitamin E (PAVE) work in treating patients with erectile dysfunction after radiation therapy for prostate cancer. Atorvastatin may reduce high cholesterol. Pentoxifylline and vitamin E may enhance blood flow. Giving PAVE may work better in treating prostate cancer patients with post-radiation therapy erectile dysfunction.

NCT ID: NCT03829930 Terminated - Clinical trials for Prostate Adenocarcinoma

Combination of Entinostat and Enzalutamide in Advanced Prostate Cancer

Start date: May 1, 2019
Phase: Phase 1
Study type: Interventional

To determine the safety and tolerability of Entinostat in combination with Enzalutamide in metastatic castrate resistant prostate cancer

NCT ID: NCT03822494 Recruiting - Prostate Cancer Clinical Trials

CyberKnife Dose Escalation Prostate Cancer Trial

CK-DESPOT
Start date: July 12, 2018
Phase: N/A
Study type: Interventional

Stereotactic body radiation therapy (SBRT) has been employed in the treatment of prostate cancer. Multiple single institution experiences suggest high biochemical control rates with acceptable toxicity in low risk prostate cancer but efficacy data in unfavorable type prostate cancer is less convincing. CyberKnife-SBRT (CK-SBRT) can be used to escalate radiation dose delivery to the prostate while sparing normal tissue.