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Interstitial Cystitis clinical trials

View clinical trials related to Interstitial Cystitis.

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NCT ID: NCT00451867 Terminated - Clinical trials for Interstitial Cystitis

A Randomized Multicenter Double-Blind CT to Evaluate the Efficacy and Safety of Mycophenolate Mofetil . . .

ICCRN RCT2
Start date: March 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the safety and effectiveness of a medication called CellCept in treating refractory (has not responded to other treatments) interstitial cystitis. CellCept belongs to a class of medications called immuno-suppressants. Immuno-suppressants work in the body by reducing the immune system's ability to produce certain reactions that can cause inflammation. In some people, the inflammation produced by their immune system can damage healthy tissues and cause symptoms of pain and discomfort. CellCept is approved by the U.S. Food and Drug Administration (FDA) for use in patients who have had an organ transplant. When used in combination with other drugs, CellCept helps to prevent the rejection of the transplanted organ and is used widely in patients who have received kidney, liver and heart transplants. CellCept is also frequently used but not FDA approved for the treatment of severe rheumatoid arthritis which is a disease caused when the body's immune system acts against healthy tissues in the joints. Due to its special activity, CellCept may be useful in treating certain inflammatory diseases or conditions like interstitial cystitis.

NCT ID: NCT00434343 Completed - Clinical trials for Interstitial Cystitis

Physical Therapy Trial for Pelvic Pain

UPPCRN-RCT#1
Start date: November 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if a randomized trial of physical therapy for pelvic pain is feasible.

NCT ID: NCT00420550 Completed - Pelvic Pain Clinical Trials

Study of Biomarkers and the Relaxation Response Using Guided Imagery in Women With IC

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

Interstitial cystitis (IC) affects more than one million women in the United States. It has been thought that IC patients who have been unable to obtain adequate relief from medical remedies would value a psychotherapeutic intervention that could diminish some of their pain. There are currently no studies using biomarkers with the use of a relaxation technique called guided imagery in IC patients. Many guided imagery intervention studies in areas such as cancer, post-operative pain, and arthritis reported that guided imagery resulted in improvements in the psychological or physiological outcomes examined. If this is also true in IC patients, this intervention may prevent the use of unnecessary medications and procedures that are currently being used.

NCT ID: NCT00389142 Recruiting - Clinical trials for Interstitial Cystitis

Identifying Genetic Causes of IC/BPS

Start date: January 15, 2006
Phase:
Study type: Observational

Interstitial cystitis (IC), also called Bladder Pain syndrome (BPS), or chronic pelvic pain syndrome(CPPS) is a common condition with no known cause or cure. Twin studies and family accounts have suggested that the condition may be genetic or passed down (inherited) from one generation to another. In this study, we are collecting genetic material and medical information from families in North America in an attempt to identify genetic factors that may cause IC/BPS/CPPS. We are enrolling families and individuals with IC/BPS/CPPS and their family members (both family members with and without IC like symptoms).

NCT ID: NCT00379002 Completed - Sexual Dysfunction Clinical Trials

The Women's Urology Center/WISH Database Project

Start date: July 2006
Phase:
Study type: Observational

Comprehensive database from the Women's Urology Center/WISH (Women's Initiative for Pelvic Pain and Sexual Health) program at Beaumont.

NCT ID: NCT00376298 Completed - Prostate Cancer Clinical Trials

Urology Database to Evaluate Clinical Information and Improve Patient Care.

Start date: February 2004
Phase: N/A
Study type: Observational

The purpose of initiating the Urology Database is to evaluate the outcomes of urology procedures and medical management to enhance the care and treatment of urology patients.

NCT ID: NCT00317070 Terminated - Clinical trials for Interstitial Cystitis

Trial Comparing Intravesical Cocktail With Intravesical Dimethyl Sulfoxide (DMSO) in Painful Bladder Syndrome/Interstitial Cystitis (PBS/IC)

Start date: April 2006
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the efficacy and tolerability of the intravesical cocktail and its comparison with intravesical DMSO in a controlled trial for the treatment of painful bladder syndrome including interstitial cystitis.

NCT ID: NCT00295854 Completed - Clinical trials for Interstitial Cystitis

Phase II Study Efficacy and Safety of Two Dosing Regimens of MN-001 in Patients With Interstitial Cystitis

Start date: May 2005
Phase: Phase 2
Study type: Interventional

To evaluate the safety and efficacy of 8 weeks of treatment with MN-001 at 500 mg bid, 500 mg once daily vs. placebo in patients with Interstitial Cystitis.

NCT ID: NCT00256542 Completed - Pelvic Pain Clinical Trials

Study of U101 for Bladder Pain and/or Urgency

Start date: January 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether intravesical U101 (alkalinized lidocaine-heparin) treatment reduces the symptoms of pelvic pain and/or urgency of bladder origin.

NCT ID: NCT00253006 Terminated - Clinical trials for Urinary Incontinence

Analysis of Expression of Nitric Oxide Syntheses and Their Functional Role in Human Urothelium

Start date: January 2006
Phase: N/A
Study type: Observational

Painful bladder syndrome (PBS)/interstitial cystitis (IC) may be due to the actions of nitric oxide (NO) in the bladder tissue. NO is a gaseous substance with a very short half-life, synthesized by a group of NO-synthase-enzymes in many tissues. The goal of this study is to illuminate bladder tissue production of NO in individuals with PBS and healthy individuals, by quantification of NO and NO-enzyme expression by different molecular biological methods.