Clinical Trials Logo

Painful Bladder Syndrome clinical trials

View clinical trials related to Painful Bladder Syndrome.

Filter by:

NCT ID: NCT02411110 Completed - Clinical trials for Painful Bladder Syndrome

A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bladder Pain Syndrome

Start date: May 21, 2015
Phase: Phase 2
Study type: Interventional

This is a safety and efficacy study of LiRIS® in females with interstitial cystitis/bladder pain syndrome.

NCT ID: NCT02232282 Completed - Clinical trials for Interstitial Cystitis

Acupuncture for Female IC/PBSyndrome and Its Effect on the Urinary Microbiome: A Randomized Controlled Trial

Start date: October 2014
Phase: N/A
Study type: Interventional

The investigators central hypothesis is that women with Interstitial Cystitis/Painful Bladder Syndrome (IC/PBS) will benefit from acupuncture compared with sham treatment and acupuncture responders will have a differential urinary microbiome.

NCT ID: NCT01294878 Completed - Clinical trials for Interstitial Cystitis

Omalizumab in Interstitial Cystitis/Bladder Pain Syndrome

IComaliz
Start date: March 2009
Phase: Phase 3
Study type: Interventional

By hypothesising that Interstitial Cystitis is an allergic disorder of the urogenital system that is linked to mast-cells, current therapy with omalizumab may represent a potential non symptomatic strategy for the treatment of IC/BPS

NCT ID: NCT01197261 Completed - Pain Clinical Trials

OXN PR vs Placebo in Opioid-naive Subjects Suffering From Severe Pain Due to Bladder Pain Syndrome (BPS)

Start date: September 2010
Phase: Phase 2
Study type: Interventional

The study compares the analgesic efficacy of OXN PR vs placebo in opioid-naive subjects suffering from severe pain due to Bladder Pain Syndrome.

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: NCT00903643 Completed - Clinical trials for Painful Bladder Syndrome

Sensory Processing in Subjects With Painful Bladder Syndrome

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

The purpose of this study is to determine if clinically relevant subsets exist in patients meeting the diagnosis of Painful Bladder Syndrome (PBS). Subsets suggest differential responses to treatments and if verified, this will be important for the stratification of patients in clinical studies related to PBS.

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: NCT00739739 Completed - Clinical trials for Interstitial Cystitis

An Effectiveness And Safety Study Of PD 0299685 For The Treatment Of Symptoms Associated With Interstitial Cystitis

Start date: August 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether PD 0299685 is effective in the treatment of symptoms associated with interstitial cystitis/painful bladder syndrome, such as pain, urinary urgency and frequency. At the same time assess the drug's safety and tolerability.

NCT ID: NCT00733603 Completed - Clinical trials for Interstitial Cystitis

Physical Therapy in Women With Interstitial Cystitis

IC03
Start date: June 2008
Phase: N/A
Study type: Interventional

There are many different treatments that doctors recommend for patients with IC/PBS. Only a few research studies have been done to evaluate treatments given to patients. Treatment choices can be of two types: drug therapy and non-drug therapy. The two treatments used in this study will be of the non-drug therapy type. One of the treatments being used in this study is called Myofascial Tissue Manipulation. This is a kind of physical therapy that is designed to work on specific muscles and tissue layers in a particular part of the body. In this study, this treatment will focus on the areas around the pelvis and the pelvic floor. The treatment will involve the physical therapist's use of hands and fingers to target specific muscles and tissues located within your pelvis, rectum, and/or vagina (the pelvic floor) as well as muscles and layers of tissue in your abdomen and legs. The other treatment being used in this study is Global Therapeutic Massage. This treatment involves the physical therapist's use of classic Western body massage techniques on the muscles of your arms, legs, hands, neck, shoulders, back, stomach, buttocks, and feet to create an overall feeling of well being. The purpose of this research study is to find out if Pelvic Physical Therapy is safe and effective on treating symptoms in women with interstitial cystitis as compared to a full body therapeutic massage. This study will also measure the lasting effects of the treatment up to 3 months after your last study treatment.

NCT ID: NCT00675298 Completed - Clinical trials for Urinary Bladder, Overactive

Linkage Analysis in Interstitial Cystitis

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

Urologic pelvic pain syndrome (UCPPS), variably termed painful bladder syndrome/interstitial cystitis (PBS/IC) in females and chronic prostatitis/chronic pelvic pain syndrome in men (CP/CPPS), is a chronic, debilitating clinical syndrome presenting as severe pelvic pain with extreme urinary urgency and frequency in the absence of any known cause. The etiologic mechanisms underlying UCPPS are unknown, but recurrence, risks to siblings of affected individuals, concordance among monozygotic twins, and our own preliminary studies indicate a strong genetic contribution to the cause of UCPPS. The overall goal of this proposal is use novel approaches to understand the basis of UCPPS, to identify candidate genes containing mutations that result in UCPPS and determine how the different encoded proteins of these genes interact with one another in a common biological pathway. Ultimately, understanding how mutations in at least five different genes yield the symptoms of UCPPS should lead to improved diagnosis and possible therapies.