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Urinary Bladder Cancer clinical trials

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NCT ID: NCT02139371 Completed - Breast Cancer Clinical Trials

Evaluation of a New Radiotracer (64Cu-DOTA-AE105) for Diagnosing Aggressive Cancer With Positron Emission Tomography

Start date: May 2014
Phase: Phase 0
Study type: Interventional

The primary objective of the study is to test a new radiotracer called 64Cu-DOTA-AE105 for PET imaging of uPAR (urokinase plasminogen activator receptor). The tracer has the potential of identifying the invasive cancer phenotype, thereby distinguishing between aggressive and less aggressive tumors. This is a first in human study to test the radiotracer in cancer patients. The biodistribution and tumor uptake will be evaluated by repeated PET imaging (1,3 and 24 hours post injection).

NCT ID: NCT01836978 Completed - Bladder Cancer Clinical Trials

Prehabilitation to Enhance Postoperative Functional Capacity Following Radical Cystectomy

Start date: June 2013
Phase: N/A
Study type: Interventional

The process of enhancing the functional capacity of an individual before an operation to enable him or her to withstand the stress of surgery has been termed prehabilitation. It has been shown that poor baseline capacity for physical performance and poor nutritional status increase the risk of complications after major non cardiac surgery and prolong recovery. A controlled randomized study in patients undergoing radical cystectomy for cancer is therefore proposed to determine the impact of multimodal prehabilitation on functional exercise capacity and functional recovery. Patients who accept to be enrolled in the study will be randomized to either a group receiving a multimodal intervention which includes nutritional supplementation (Immunocal® whey protein) combined with a physical exercise program and stress reduction strategies before and after surgery, or a control group who will receive standard preoperative treatment as per our institution.

NCT ID: NCT00462488 Completed - Bladder Cancer Clinical Trials

Study of Vicinium for Treating Patients With Non-Invasive Urothelial Carcinoma In Situ

Start date: March 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and tolerability of Vicinium when administered as a monotherapy intravesical instillation in patients with non-invasive urothelial carcinoma in situ (CIS) who failed previous treatment with Bacille Calmette Guérin (BCG).