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Interstitial Cystitis clinical trials

View clinical trials related to Interstitial Cystitis.

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NCT ID: NCT02514265 Completed - Clinical trials for Interstitial Cystitis

Trans-MAPP Symptom Patterns Study (SPS)

MAPP II SPS
Start date: July 1, 2015
Phase:
Study type: Observational

This study is the second phase of the MAPP Network and is designed to conduct a prospective, observational study of men and women with UCPPS, referred to as the Symptom Patterns Study (SPS), enriched with pre-defined subgroups, with longer follow-up, in order to further investigate clinical and biologic factors associated with worsening and/or improvement of reported urinary and non-urinary symptoms.

NCT ID: NCT02457182 Completed - Clinical trials for Interstitial Cystitis

Mindfulness-Based Therapy for Interstitial Cystitis/Bladder Pain Syndrome

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

Interstitial cystitis/bladder pain syndrome (IC/BPS) is a poorly understood disease with unreliable treatments. Although it is not known what causes it for certain, we do know that life stressors may make the disease worse or cause flares. Mindfulness Based Stress Reduction (MBSR) is an 8 week class focused on meditation and other techniques that the investigators think may be helpful to people with IC/BPS. This trial will assign participants to an MBSR class or usual care for their IC/BPS to see if the MBSR class would be helpful for their disease.

NCT ID: NCT02297100 Completed - Clinical trials for Interstitial Cystitis

Intravesicular Onabotulinumtoxin A in Interstitial Cystitis

Start date: December 2014
Phase: Phase 4
Study type: Interventional

The purpose of this research study is to identify the optimal usage of Onabotulinumtoxin A in interstitial cystitis. Onabotulinumtoxin A, more commonly known by the trade name Botox®, is a medication that comes from the bacteria Clostridium botulinum. It works by blocking the release of the neurotransmitter acetylcholine(a chemical messenger that carries signals between nerve cells and other cells in the body). Blocking that neurotransmitter results in decreased muscle activity.

NCT ID: NCT02247557 Completed - Clinical trials for Interstitial Cystitis

Intravesical Instillation of Liposome Encapsulated Botulinum Toxin A (Lipotoxin) in Treatment of Interstitial Cystitis

Start date: September 2014
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and safety of intravesical instillation of Lipotoxin for the treatment of IC/BPS

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: NCT02150811 Completed - Clinical trials for Interstitial Cystitis

Observational Study of Hunner's Ulcer in Patient With Interstitial Cystitis/Bladder Pain Syndrome

Start date: June 2, 2016
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to observe change of distribution pattern of Hunner's ulcer in patient with interstitial cystitis/bladder pain syndrome

NCT ID: NCT02000401 Completed - Clinical trials for Interstitial Cystitis

Intranasal Ketorolac Tromethamine (Sprix) for Acute Pain of Interstitial Cystitis Flare of Pain

Start date: May 2012
Phase: Phase 4
Study type: Interventional

Intranasal Ketorolac tromethamine has a potential role as a short term pain management tool for Interstitial Cystitis without the risk and undesirable effects of narcotics.

NCT ID: NCT01997983 Completed - Clinical trials for Interstitial Cystitis

Efficacy and Safety of Intravesical Instillations of Botulinum Toxin in TC-3 Gel in IC Patients

Start date: November 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The investigators believe that this study is of importance of several aspects: 1. It evaluates a new mode of bladder instillation that may bypass the drawbacks of the current instillation mode. 2. It will demonstrating safety of intravesical instillations of BTX mixed with TC-3 gel in IC patients 3. If proved effective or partially effective, this mode of treatment will serve as a basis for large feasibility study exploring its safety and efficacy aspects.

NCT ID: NCT01990898 Completed - Clinical trials for Interstitial Cystitis

Cyclosporine in Interstitial Cystitis: Efficacy, Safety and Mechanism of Action

CIC
Start date: November 2013
Phase: Phase 2
Study type: Interventional

This is a study for patients that have a condition called Interstitial Cystitis, also known as Painful Bladder Syndrome. Patients would have tried at least two different therapies, unsuccessfully,(eg. medications, pelvic floor physical therapy) The purpose of this research project is to study the immunosuppressive drug Cyclosporine in patients with Interstitial Cystitis to assess how well it works, what the side effects are and what is its mechanism of action. Cyclosporine is a drug that is FDA-approved to prevent organ rejection after kidney, liver, and heart transplant but is not approved by the FDA for Interstitial Cystitis. Several research studies have been published showing that Cyclosporine can improve the symptoms of Interstitial Cystitis, that it works better than a placebo ("sugar pill" or inert treatment) and that it works more effectively than Pentosan Polysulfate (Elmiron), which is an FDA approved therapy. The dose of Cyclosporine used in these studies on Interstitial Cystitis are much lower that the doses used to prevent rejection in transplant patients. Based on these studies, the American Urological Association has recently published treatment guidelines that recommend Cyclosporine therapy for Interstitial Cystitis after the failure of other more conservative therapies and medications. Nevertheless, much is not known about using Cyclosporine therapy for Interstitial Cystitis including the mechanism of action, the ideal dose, how best to monitor for side effects and in particular whether kidney damage can occur at the low doses used in these studies. In this study, to examine the mechanism of action, blood and urine samples will be collected before, during and after therapy to look at "biomarkers", chemical substances that can be associated with inflammation and tissue injury. We will also test effects of therapy on skin sensation and pain perception because the molecule which Cyclosporine binds to (calcineurin) is also found in nerves that conduct pain signals. This study is only being done at the Cleveland Clinic and will involve about 30 patients with Interstitial Cystitis.

NCT ID: NCT01985880 Completed - Clinical trials for Interstitial Cystitis

The Efficacy of Biomarker in Patient With Interstitial Cystitis/Painful Bladder Syndrome

Start date: November 19, 2013
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to evaluate efficacy of biomarker in patient with interstitial cystitis/painful bladder syndrome