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Cystitis, Interstitial clinical trials

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NCT ID: NCT02743962 Completed - Clinical trials for Painful Bladder Syndrome

A Pilot Study Investigating the Use of a Therapeutic Wand in Addition to Physiotherapy for Bladder Pain Syndrome

Start date: April 2016
Phase: N/A
Study type: Interventional

Bladder pain syndrome is a condition where pain is experienced when the bladder fills with urine and eases briefly when the bladder empties. There can also be a constant need to urgently empty the bladder. The internal pelvic floor muscles in people with bladder pain syndrome can be tense and painful, and relaxing and stretching them may improve symptoms; reducing bladder pain, urgency and how often people have to empty their bladder. This pelvic floor release is done by specialist physiotherapists.Therapeutic wands, such as the TheraWand®, are used routinely throughout the United Kingdom to allow people to relax and stretch their pelvic floor themselves. Using a therapeutic wand has been shown to be safe and to reduce pelvic pain, improve bladder and bowel symptoms and relax the pelvic floor muscles. However, this research was conducted mostly in men with pelvic pain. The aim of this study is to find out if using a therapeutic wand at home as well as having a specialist physiotherapist massage the pelvic floor gives any added benefit than just having the physiotherapy treatment. The investigators hope to find out if the therapeutic wand gives women a way of managing their symptoms independently in their own homes.

NCT ID: NCT02600715 Completed - Overactive Bladder Clinical Trials

Reduction of Bladder Injection Pain With Belladonna Opiate Suppository

ROBIN
Start date: November 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to test whether using belladonna & opiate suppositories (B&Os) can improve patient discomfort during Onabotulinumtoxin A (BoNT) injection into the bladder for treatment of overactive bladder, neurogenic detrusor overactivity, or interstitial cystitis.

NCT ID: NCT02550561 Completed - Clinical trials for Interstitial Cystitis

Pilot Study of Percutaneous Posterior Tibial Nerve Stimulation for the Treatment of IC/PBS

Start date: June 2015
Phase: N/A
Study type: Interventional

In 2014, the American Urological Association updated it management algorithm for Interstitial Cystitis/Painful Bladder Syndrome (IC/PBS). As the algorithm progresses, interventions become increasingly invasive and morbid. 4th line treatment is sacral neuromodulation (SNM), involving a two stage surgical procedure and permanent device implantation. While the mechanism for decrease in IC/PBS symptoms is unknown, SNM is thought act through central and peripheral mechanisms related to afferent signaling, causing modification of pain and lower urinary tract sensation.¹ Percutaneous posterior tibial nerve stimulation (PTNS) is a method of peripheral neuromodulation targeting the same nerve roots as SNM, but with significantly fewer risks. The purpose of our research is to determine if PTNS is effective in the treatment of IC/PBS. The results of this study will suggest future directions and provide critical information to design studies to determine to what extent and in what situations PTNS may be effective. The investigators will enroll subjects with IC/PBS and urinary frequency/urgency to treatment with 12 weekly treatments of PTNS. The investigators will assess symptoms and lower urinary tract function before, during and after the treatments. At the completion of treatments, subjects will be asked to enroll in post-study follow up monitoring to understand the duration of symptom effect.

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: NCT02497976 Completed - Clinical trials for Cystitis, Interstitial

Pilot Study Evaluating the Efficacy of Certolizumab Pegol for Interstitial Cystitis

Start date: December 15, 2015
Phase: Phase 3
Study type: Interventional

A Randomized, Double-blind, Placebo Controlled Trial of Certolizumab Pegol in Women with Refractory Interstitial Cystitis/Bladder Pain Syndrome

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: 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: NCT02395042 Completed - Ulcer Clinical Trials

A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis With Hunner's Lesions

Start date: April 15, 2015
Phase: Phase 2
Study type: Interventional

This is a safety and efficacy study of LiRIS® in females with interstitial cystitis with Hunner's lesions.

NCT ID: NCT02331472 Completed - Clinical trials for Chronic Interstitial Cystitis

The Efficacy of Urine Biomarker in Patient With Interstitial Cystitis/Painful Bladder Syndrome (Pilot Study)

Start date: February 3, 2015
Phase:
Study type: Observational [Patient Registry]

This study is to evaluate the efficacy of urine biomarker in patients with interstitial cystitis/painful bladder syndrome

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.