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Bladder Cancer clinical trials

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NCT ID: NCT00578526 Completed - Bladder Cancer Clinical Trials

SU011248 for Platinum-Refractory Urothelial Cancer Evaluation Trial

SPRUCE
Start date: April 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to find out if SU011248 works and if it is safe in patients with advanced transitional cell carcinoma.

NCT ID: NCT00578006 Completed - Breast Cancer Clinical Trials

Internet-based System for Cancer Patients to Self-report Toxicity

Start date: March 2004
Phase: N/A
Study type: Interventional

Cancer patients may develop side effects during treatment, such as nausea, pain, fatigue, diarrhea, constipation, or shortness of breath. These symptoms may be due to the cancer itself, or due to treatments like chemotherapy drugs or radiation therapy. Doctors and nurses often ask patients about their symptoms, because an important part of cancer treatment is to make patients feel as well as possible. If patients do not feel well, the investigators may need to change the way the investigators are treating you or prescribe therapies that will decrease your symptoms. The best way to find out how you are feeling is to ask you directly. However, during your time between appointments the investigators may not be able to ask you how you are feeling on a regular basis. In addition, even at an appointment, there may be symptoms that the investigators do not have a chance to discuss. The investigators are interested in developing new ways to ask patients about how they are feeling, using the Internet. A special new website called STAR ("Symptom Tracking and Reporting for Patients") has been developed to help patients record this information, so that their doctors and nurses can review it during clinic appointments. This study is designed to help us see if STAR is a helpful way for us to keep track of information about patients' symptoms and quality of life.

NCT ID: NCT00567684 Active, not recruiting - Bladder Cancer Clinical Trials

Computed Tomography Urography (CTU) vs Intravenous Urography (IVU) on Patients at Risk of Urothelial Tumors

Start date: November 15, 2007
Phase: N/A
Study type: Interventional

The goal of this clinical research study is to use computed tomography urography (CTU) scans and intravenous urography (IVU) scans to check the status of urothelial cancer, in order to try to learn the level of effectiveness of possibly using CTU by itself in future patients.

NCT ID: NCT00565227 Terminated - Prostate Cancer Clinical Trials

Phase I Study of Vorinostat in Combination With Docetaxel in Patients With Advanced and Relapsed Solid Malignancies.

Start date: April 2007
Phase: Phase 1
Study type: Interventional

Vorinostat (Suberoylanilide Hydroxamic Acid; NSC 701852) is a drug that inhibits an enzyme that plays a key role in the regulation of cell survival, growth, and eventual cell death, all of which play a role in cancer. As a result, this drug has the potential to affect a tumor's ability to survive. Vorinostat is the most potent drug of its kind that is currently under investigation in clinical trials. The primary objective of this study is to define the maximum safest dose of vorinostat in combination with a standard chemotherapy agent, docetaxel, in patients with advanced and relapsed lung, bladder, or prostate cancer.

NCT ID: NCT00556621 Completed - Bladder Cancer Clinical Trials

Gemcitabine, Cisplatin, and Radiation Therapy in Treating Patients With Stage II or Stage III Bladder Cancer

GEMCIRAV
Start date: June 2005
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as gemcitabine and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving combination chemotherapy together with radiation therapy may kill more tumor cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of gemcitabine when given together with cisplatin and radiation therapy and to see how well they work in treating patients with stage II or stage III bladder cancer.

NCT ID: NCT00553566 Recruiting - Bladder Cancer Clinical Trials

Effect of Dietary, Lifestyle, and Environmental Factors on Patients With Early-Stage Bladder Cancer

Start date: December 2005
Phase: Phase 3
Study type: Observational

RATIONALE: Learning about the long-term effects of dietary, lifestyle, and environmental factors on the risk of cancer progression and recurrence may help the study of bladder cancer in the future. PURPOSE: This clinical trial is studying how dietary, lifestyle, and environmental factors affect patients with early-stage bladder cancer.

NCT ID: NCT00553345 Recruiting - Bladder Cancer Clinical Trials

Selenium and Vitamin E in Preventing Cancer Progression and Recurrence in Patients With Early-Stage Bladder Cancer

Start date: December 2005
Phase: Phase 3
Study type: Interventional

RATIONALE: Chemoprevention is the use of certain drugs to keep cancer from forming. The use of selenium and vitamin E may stop cancer from growing or coming back. PURPOSE: This randomized phase III trial is studying giving selenium together with vitamin E to see how well it works compared with a placebo in preventing cancer progression and recurrence in patients with early-stage bladder cancer.

NCT ID: NCT00553215 Recruiting - Bladder Cancer Clinical Trials

Quality of Life in Patients With Bladder Cancer

Start date: December 2005
Phase: Phase 3
Study type: Observational

RATIONALE: Studying quality of life in patients with bladder cancer may help determine the long-term effects of bladder cancer and may help improve the quality of life for patients in the future. PURPOSE: This clinical trial is studying quality of life in patients with bladder cancer.

NCT ID: NCT00553124 Recruiting - Bladder Cancer Clinical Trials

Different Factors Affecting Patients With Newly Diagnosed Bladder Cancer

Start date: December 2005
Phase: Phase 3
Study type: Interventional

RATIONALE: Studying different factors that effect patients with newly diagnosed bladder cancer may help doctors learn more about the disease, improve the ability to plan cancer treatment, and help patients live more comfortably. PURPOSE: This clinical trial is studying different factors affecting patients with newly diagnosed bladder cancer.

NCT ID: NCT00544609 Completed - Bladder Cancer Clinical Trials

Sorafenib and Radiotherapy in the Treatment of Invasive Bladder Cancer With Conservative Intent

SOGUG-07-01
Start date: December 2007
Phase: Phase 1
Study type: Interventional

Safety profile and to determine maximum tolerated dose of Sorafenib in combination with Radiotherapy in the Treatment of Invasive Bladder Cancer With Conservative Intent