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Cystitis clinical trials

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NCT ID: NCT00958295 Completed - Clinical trials for Acute Uncomplicated Bacterial Cystitis

Epidemiology of Acute Bacterial Uncomplicated Cystitis in General Practice

BaCyst
Start date: March 2009
Phase: N/A
Study type: Observational

Acute uncomplicated bacterial cystitis is common in general practice. Cystitis is at the second raw of antibiotic treatment indications. It has been now recommended not to perform any urine culture for more than 20 years; hence, the bacterial epidemiology of acute uncomplicated cystitis is surprisingly relatively unknown. The available bacteriological data mainly describe the epidemiology of complicated urinary tract infections or upper urinary tract infections, but the causative bacteria and the resistance rates might differ from those of uncomplicated cystitis. As an example, it is unknown to what extent Staphylococcus saprophyticus is the causative agent of uncomplicated cystitis. Moreover, the urine dipstick test have been evaluated in laboratories. But their interpretation in current practice might not be so easy: in particular, the nitrite detection depends on the bacterial concentration. The nitrite detection, produced in enterobacteriaceae related infections might have therapeutical consequences: trométamol-fosfomycine is almost constantly active on enterobacteriaceae, but ineffective on staphylococci. Knowing the increasing prevalence of fluoroquinolone-resistant enterobacteriaceae, the use of fosfomycin in nitrite positive uncomplicated cystitis might preserve the susceptibility of fluoroquinolones during pyelonephritis. This study will describe: - the bacterial epidemiology of acute uncomplicated cystitis in general practice, - the correlation in between urine dipstick and urine culture in general practice, - the prediction of enterobacterial infection by the nitrite detection, AND - the antibiotics prescribed by the practitioners for uncomplicated acute cystitis.

NCT ID: NCT00957333 Completed - Cystitis Clinical Trials

Effects of Ketamine on Human Bladders and Its Possible Mechanisms

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

This study is aimed to evaluate the relationship between ketamine abused and bladder dysfunction and its possible mechanisms.

NCT ID: NCT00919802 Completed - Clinical trials for Interstitial Cystitis

Intranasal Oxytocin for the Treatment of Pain Associated With Interstitial Cystitis

Start date: June 2010
Phase: N/A
Study type: Interventional

Anecdotal evidence suggests female patients with painful bladder disorder interstitial cystitis (IC) can experience a significant attenuation of their systems while breastfeeding. Since it has been shown that postpartum lactation is a time associated with decreased levels of stress, and stress has been shown to exacerbate IC-related pain, the investigators have developed an interest in the effects of the hormones involved in postpartum lactation on stress and pain. Based on a series of pre-clinical experiments, the investigators believe the hormone oxytoxin has both analgesic and anxiolytic properties which make it a potentially useful agent for the treatment of stress-exacerbated chronic pain syndrome such as IC. Therefore, the investigators propose a double-blinded, placebo-controlled crossover trial of intranasal oxytocin vs. intranasal saline for bladder pain in a cohort of patients with IC and some degree of continuous, daily pain.

NCT ID: NCT00919113 Completed - Clinical trials for Interstitial Cystitis

Efficacy and Safety Study of Uracyst to Treat Interstitial Cystitis/Painful Bladder Syndrome

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

A new device for interstitial cystitis is compared to inactive control to determine if it is safe and effective. The study lasts approximately 7 weeks with a 19-week follow-up period.

NCT ID: NCT00903435 Completed - Clinical trials for Interstitial Cystitis

Quantitative Studies of Urinary Bladder Sensation

Start date: May 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether more than one subpopulation exists of patients with the diagnosis of Interstitial Cystitis (IC) based on sensory testing and to determine if subjects with IC have normal counterirritation-related modulatory systems.

NCT ID: NCT00873171 Completed - Clinical trials for Interstitial Cystitis

Osteopathic Manipulation Therapy in the Treatment of Interstitial Cystitis

Start date: January 2009
Phase: N/A
Study type: Observational

As a safe and noninvasive method of treatment, the intent of the study is to show that Osteopathic manipulation therapy is a beneficial treatment for the aggravating bladder symptoms seen in all patients with interstitial cystitis.

NCT ID: NCT00817388 Completed - Pelvic Pain Clinical Trials

Correlating Ic/Pbs Symptoms With Urine Biomarkers

Start date: January 2009
Phase: N/A
Study type: Observational

Completion of a brief survey tool and providing an urine specimen. The study purpose is to improve our understanding of interstitial cystitis and painful pelvic syndrome.

NCT ID: NCT00801021 Completed - Clinical trials for Urinary Tract Infections

Treatment and/or Prevention of Urinary Tract Infections

UTI
Start date: December 2008
Phase: Phase 1
Study type: Interventional

The purpose of the study is to determine the effect of an investigational oral rinse in reducing uropathogens and treating uncomplicated urinary tract infections.

NCT ID: NCT00775281 Completed - Overactive Bladder Clinical Trials

Changes in Inflammatory and Contractile Protein Expression in Patients With Painful Bladder Syndrome/IC.

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

Interstitial cystitis (IC)/chronic pelvic pain syndrome (CPPS) is a clinical syndrome of pelvic pain and/or urinary urgency/frequency in absence of a specific cause such as bacterial infection or damage to the bladder. The pathogenetic mechanisms of IC/CPPS are as yet undefined and it is largely this lack of knowledge, which precludes a systematic therapeutic approach. Experimental evidence, including results from the animal models of cystitis and the knock-out mice, indicate a participation of tachykinin receptors, especially the NK1R, in neurogenic inflammation, which is considered an important element of the IC complex. However, there is very scant information about the molecular mechanisms of IC in humans, or of the types of receptors, which participate in neurogenic inflammation. Based on our molecular biological know-how and the clinical expertise, we propose to investigate the role of the tachykinin and bradykinin receptors and their signalling partners in CPPS and bladder dysfunction in humans.

NCT ID: NCT00751010 Completed - Vulvodynia Clinical Trials

Relationship: Interstitial Cystitis & Vulvodynia-Part 2

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

The etiology of pain in women with IC is often difficult to identify resulting in unnecessary medical and surgical treatments (e.g. hysterectomies). The vulva may actually be the site of some of the reported pain in women with IC, not the urethra or bladder. IC and vulvodynia can impact one's sexual functioning and diminish one's quality of life. Unfortunately, vulvodynia is often unrecognized since it is not part of the usual urological assessment with IC patients. Vulvodynia is characterized by persistent generalized or localized vulvar pain of varying degrees often characterized as "burning," suggestive of a neuropathic pain response.