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Bladder Cancer clinical trials

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NCT ID: NCT01082510 Recruiting - Bladder Cancer Clinical Trials

Study of the Efficacy of Maintenance Therapy Using Uracil-tegafur (UFT) or Bacille Calmette-Guerin (BCG) for the Prevention of Recurrences of Superficial Bladder Cancer (EMBARK Study)

Start date: January 2010
Phase: Phase 3
Study type: Interventional

The purpose of this prospective randomized controlled study is to prove the non-inferiority of UFT maintenance therapy to BCG maintenance therapy for preventing recurrences of superficial bladder cancer.

NCT ID: NCT01076387 Completed - Bladder Cancer Clinical Trials

Randomized Trial Comparing Robotic and Open Radical Cystectomy

Start date: February 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if using robotic surgical technology during bladder cancer surgery helps to reduce complications during and after the surgery. The removal of the bladder and lymph nodes will be done by a robotic or by an open technique. It may be a Robotic-assisted Radical Cystectomy (RARC) and Pelvic Lymph Node Dissection. Or it may be an Open Radical Cystectomy (ORC) and Pelvic Lymph Node Dissection.

NCT ID: NCT01060319 Withdrawn - Bladder Cancer Clinical Trials

A Comprehensive Study to Isolate Tumor-initiating Cells From Human Epithelial Malignancies

Start date: December 2013
Phase:
Study type: Observational

We hypothesize that all human malignancies harbour a subpopulation of tumor initiating cells/cancer stem cells (CSCs) that drives tumor development and potentially recurrence or metastasis of the disease. The primary aim of this study is to develop strategies for prospective isolation/enrichment of CSCs from human tumors of different tissue origins. In addition, we will characterize the signaling pathways and/or tumor specific antigens that are specific for CSCs, in order to specifically target these CSCs as the endpoint of this study.

NCT ID: NCT01042795 Terminated - Bladder Cancer Clinical Trials

Trial of Adjuvant Sutent for Patients With High Risk Urothelial Carcinoma After Neoadjuvant Chemotherapy and Cystectomy

Start date: September 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether sutent (sunitinib)is effective in preventing tumor recurrence in patients with high risk bladder cancer who have previously had chemotherapy and cystectomy (bladder removal). A 4 month supply of the drug is given to patients beginning 2-3 months after bladder removal. The patients are followed up to 2 years.

NCT ID: NCT01031875 Completed - Bladder Cancer Clinical Trials

Pazopanib Hydrochloride in Treating Patients With Metastatic Urethral Cancer or Bladder Cancer That Has Relapsed or Not Responded to Treatment

Start date: December 2009
Phase: Phase 2
Study type: Interventional

RATIONALE: Pazopanib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. PURPOSE: This phase II trial is studying how well pazopanib hydrochloride works in treating patients with or metastatic urothelial cancer or bladder cancer that has relapsed or not responded to treatment.

NCT ID: NCT01015963 Completed - Breast Cancer Clinical Trials

Studying DNA in Tissue Samples From Caucasian and African-American Cancer Patients Who Received Docetaxel on Clinical Trial CLB-9871

Start date: October 2008
Phase: N/A
Study type: Observational

This research trial studies deoxyribonucleic acid (DNA) in blood samples from Caucasian and African-American cancer patients who received docetaxel on clinical trial CLB-9871. Studying samples of blood from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors learn more about how docetaxel is used by the body.

NCT ID: NCT01010334 Terminated - Lung Cancer Clinical Trials

Comparison of Standard of Care or Treatment on Protocol

Start date: March 2009
Phase: N/A
Study type: Interventional

Patient will choose to either receive the standard of care according to National Comprehensive Cancer Network (NCCN) or approved guidelines for their condition or to be treated according to one arm of the protocol that they could not be enrolled on. The selection of the arm will be at physician discretion.

NCT ID: NCT01008865 Completed - Bladder Cancer Clinical Trials

A Comparison of the Studer Pouch Versus the T-Pouch Orthotopic Neobladder Urinary Diversion in Bladder Cancer Patients

Start date: January 4, 2002
Phase: N/A
Study type: Interventional

This is a prospective, randomized study of two types of continent ileal neobladder construction in patients undergoing cystectomy for primary bladder cancer. Patients will be randomly assigned to have either a T-pouch or a Studer pouch constructed at the time of their surgery. They will be followed long-term to determine the relative advantages and disadvantages of the two types of diversion. The investigators' hypothesis is that the inclusion of an antireflux mechanism in the T-pouch will result in significantly fewer episodes of symptomatic urinary tract infection, and will have a lower incidence of upper tract dilation and loss of renal function over the long term.

NCT ID: NCT01007058 Completed - Bladder Cancer Clinical Trials

Markers of Response to Intravesical Bladder Cancer Therapy

Start date: June 2005
Phase: N/A
Study type: Observational

The goal of this laboratory research study is to see if researchers can predict whose cancer will stay in remission and whose will return in patients receiving treatment for bladder cancer.

NCT ID: NCT01000129 Recruiting - Bladder Cancer Clinical Trials

Adaptive Planning in Bladder Cancer

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Start date: January 2009
Phase: Phase 2
Study type: Interventional

To demonstrate that radiotherapy treatments for bladder cancer can be delivered with greater accuracy using a new planning method and that this method can be used simply and effectively by those delivering treatment.