Chronic Interstitial Cystitis

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Review clinical trials related to Chronic Interstitial Cystitis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Investigation of PEMF Therapy for Female Patients With IC/BPS

The purpose of this study is to gather information about the safety and effectiveness of the non-pharmacological (non-drug), non-invasive treatment known as low-frequency pulsed electromagnetic field (PEMF) therapy. The study team will distribute the PEMF device to female adults with Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) to measure its ability to decrease bladder and pelvic pain as well as other urinary symptoms associated with IC/BPS. There are two sequential Aims in this study and subjects will be recruited to participate in only one Aim. In both Aims, data will be collected at baseline/enrollment, 4-weeks after using PEMF therapy, and 8, 12, and 16 weeks post-enrollment.

Participants needed: 75
Trial details
Age: 18-80Biological sex: FemaleType: InterventionalSponsor: Wake Forest University Health SciencesUpdated: May 7, 2026Locations: 1
Eligibility criteria

Previously established clinical diagnosis of IC/PS [+3]

History of bladder, ovarian, vaginal cancer [+9]

Status: Not yet recruiting

Efficacy of Pulsed Electromagnetic Field and Heparin/Bupivacaine Instillations

The objective of this study is to test the idea that Pulsed Electromagnetic Field (PEMF) therapy will serve as a safe therapeutic modality that can effectively be administered simultaneously with bladder instillations of a bupivacaine-heparin cocktail to improve the chronic pain and/or associated symptoms of Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) patients. The study team will distribute the PEMF device to female adults with IC/BPS who have been prescribed bladder instillations of bupivacaine-heparin to see if PEMF therapy in conjunction with bladder instillations of heparin and bupivacaine may be more effective in reducing pain levels and symptomatology of IC/BPS than instillations alone.

Participants needed: 20
Trial details
Age: 18-80Biological sex: FemaleType: InterventionalSponsor: Wake Forest University Health SciencesUpdated: Mar 31, 2026Locations: 1
Eligibility criteria

Previously established clinical diagnosis of Interstitial Cystitis/Bladder Pain... [+4]

History of bladder, ovarian or vaginal cancer [+13]

Status: Recruiting

Pain Type and Interstitial Cystitis/Bladder Pain Syndrome Treatment

Interstitial cystitis/bladder pain syndrome (IC/BPS) is a severe pain condition affecting 3-8 million people in the United States lacking treatments that work. Emotional suffering is common in IC/BPS and known to make physical symptoms worse, and studies show patient sub-groups respond differently to treatment. Individuals with IC/BPS have distinct subgroups, or "phenotypes," largely characterized by the distribution of pain throughout the body. Supported by our preliminary evidence, the overall goal of this project is to assess how IC/BPS phenotype may affect response to two different therapies often given without regard to patient phenotype, pelvic floor physical therapy (PT) and cognitive-behavioral therapy (CBT) for IC/BPS.

Participants needed: 220
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Vanderbilt University Medical CenterUpdated: Jan 21, 2026Locations: 1
Eligibility criteria

18 years of age or older; [+3]

Comorbid neurological conditions including spinal cord injury or systematic neur... [+12]

Status: Recruiting

Safety and Efficacy of Aloe Vera in the Management of the Symptoms of Interstitial Cystitis

The purpose of this study is to assess the safety and efficacy of super-concentrated, freeze-dried aloe vera capsules for treatment of interstitial cystitis.

Participants needed: 30
Trial details
Phase: Early Phase 1Age: 18-80Biological sex: AllType: InterventionalSponsor: Wake Forest University Health SciencesUpdated: Aug 27, 2025Locations: 1
Eligibility criteria

Females or males, aged 18 years or older [+6]

Known allergy or intolerance to aloe vera in any form as reported by the partici... [+21]