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Ileal Conduit clinical trials

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NCT ID: NCT06190197 Not yet recruiting - Clinical trials for Muscle-Invasive Bladder Carcinoma

Prophylactic Antibiotics in Cystectomy With Diversion

Start date: April 15, 2024
Phase: Early Phase 1
Study type: Interventional

Using a randomized 2 arm design, this study is being conducted to test for non-inferiority of no prophylactic antibiotic therapy versus the prophylactic oral antibiotic, nitrofurantoin, through comparison of rates of postoperative urinary tract infections within the 90-day postoperative period in patients with muscle invasive bladder cancer who undergo radical cystectomy with urinary diversion.

NCT ID: NCT06032910 Recruiting - Bladder Cancer Clinical Trials

Surgical Mesh in Radical Cystectomy to Prevent Parastomal Hernias

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

Radical cystectomy with ileal conduit urinary diversion serves as a foundational curative treatment strategy for selected patients afflicted with urothelial carcinoma of the bladder. Parastomal hernia after this procedure is an underestimated and undertreated clinical entity, which heavily impairs patients' quality of life due to symptoms of pain, leakage, application or skin problems. There is little evidence about prophylactic mesh placement for parastomal hernia prevention. In this study we examine the use of meshes during radical cystectomy and compare them with a control group.

NCT ID: NCT04055311 Recruiting - Bladder Cancer Clinical Trials

Recovery Support for Bladder Cancer Patients and Caregivers

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

For patients with certain types of bladder cancer, the removal of the bladder and the construction of an artificial bladder or reservoir are the only treatment options. Both before and after treatment, patients and caregivers face profound challenges preparing for surgery and planning for tasks during their recovery. To aid in recovery and enhance quality of life this program of research will develop and evaluate a multi-stage intervention geared towards patients and their caregivers. Part 1 of this program will have a nurse or trained health professional prepare both patients and their caregivers before treatment about the upcoming surgery. During this time the nurse will also demonstrate the necessary tools and techniques for stoma care. In addition, patients and their caregivers will receive access to a recovery website, specifically designed for bladder cancer patients to be used as a resource for after treatment. The website will be part 2 of this research and will contain important recovery information, videos about post-surgical care, testimonials by other patients and physicians and a variety of other resources. Patients and caregivers in the control group will receive the Facing Forward brochures from the National Cancer Institute in part 2. This research has been funded by the National Cancer Institute and will be the first study to address the needs of bladder cancer patients and their caregivers. The ultimate goal of the study is to reduce infections and unplanned nurse/ER visits and improve quality of life for both patients and their caregivers. This new program will be evaluated over the course of 12-months and if found successful, has the potential to be disseminated throughout the health care systems of the two study sites.

NCT ID: NCT03280459 Recruiting - Clinical trials for Urothelial Carcinoma

Evaluation of Robot-assisted Intracorporeal Urinary Reconstruction

iRARC-KSW
Start date: January 1, 2015
Phase: N/A
Study type: Observational [Patient Registry]

Continous evaluation of clinical and oncologic outcome of robot-assisted cystectomy with intracorporeal reconstruction of urinary diversion. Patient Data is entered in an anonymized registry for analyzation.

NCT ID: NCT02387333 Recruiting - Parastomal Hernia Clinical Trials

Role of Mesh Stoma Reinforcement Technique (MSRT) in Prevention of Parastomal Hernia After Ileal Conduit Urinary Diversion

Start date: February 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this clinical trial is to investigate the safety and efficacy of prophylactic mesh on prevention of parastomal hernia(PSH) after ileal conduit urinary diversion (IC) in a randomized controlled fashion.