Interstitial Cystitis Clinical Trial
Official title:
Cyclosporine in Interstitial Cystitis: Efficacy, Safety and Mechanism of Action
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.
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.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04313972 -
IC PaIN Trial: Interstitial Cystitis Pain Improvement With Naltrexone
|
Phase 4 | |
Completed |
NCT03282318 -
A Study to Investigate Efficacy, Safety, Pharmacodynamics and Pharmacokinetics of ASP6294 in the Treatment of Female Subjects With Bladder Pain Syndrome/Interstitial Cystitis
|
Phase 2 | |
Completed |
NCT03463499 -
The Efficacy and Safety of Intravesical Hyaluronic Acid and Chondroitin Sulfate After Transurethral Resection of Hunner Lesion in Interstitial Cystitis/Bladder Pain Syndrome Patients
|
N/A | |
Completed |
NCT02898220 -
Trans-MAPP II Study of Urologic Chronic Pelvin Pain
|
||
Terminated |
NCT02591199 -
Engage 24: Evaluation of the Safety and Effectiveness of URG101 in Subjects With Interstitial Cystitis/Bladder Pain Syndrome
|
Phase 2 | |
Completed |
NCT02247557 -
Intravesical Instillation of Liposome Encapsulated Botulinum Toxin A (Lipotoxin) in Treatment of Interstitial Cystitis
|
Phase 2 | |
Active, not recruiting |
NCT01731470 -
Intravesical Liposomes for Interstitial Cystitis/Painful Bladder Syndrome (IC/PBS)
|
N/A | |
Completed |
NCT01197261 -
OXN PR vs Placebo in Opioid-naive Subjects Suffering From Severe Pain Due to Bladder Pain Syndrome (BPS)
|
Phase 2 | |
Completed |
NCT00971568 -
Urinary Biomarkers Characteristic to Interstitial Cystitis
|
N/A | |
Completed |
NCT00527917 -
A Pilot Clinical Investigation of the Efficacy and Safety of Uracyst® Versus Placebo in Patients With Interstitial Cystitis/Painful Bladder Syndrome.
|
Phase 2 | |
Completed |
NCT00150488 -
URACYST® For the Treatment of GAG Deficient Interstitial Cystitis
|
N/A | |
Recruiting |
NCT00094874 -
Acupuncture for the Treatment of Interstitial Cystitis (IC) Symptoms
|
Phase 3 | |
Terminated |
NCT00086684 -
Effectiveness and Safety Study of Pentosan Polysulfate Sodium for the Treatment of Interstitial Cystitis
|
Phase 4 | |
Recruiting |
NCT04845217 -
Peppermint Oil for the Treatment of Interstitial Cystitis / Bladder Pain Syndrome
|
Phase 1/Phase 2 | |
Completed |
NCT04401176 -
Bladder Instillations Versus Onabotulinumtoxin A for Treatment of Interstitial Cystitis/Bladder Pain Syndrome
|
Phase 2 | |
Recruiting |
NCT05147779 -
Safety of Cultured Allogeneic Adult Umbilical Cord Stem Cells for Peyronie's Disease, ED, and Interstitial Cystitis
|
Phase 1 | |
Suspended |
NCT04450316 -
Low-dose Naltrexone for Bladder Pain Syndrome
|
Phase 2 | |
Completed |
NCT04010513 -
Hypnosis for Bladder Pain Syndrome
|
N/A | |
Completed |
NCT05179460 -
A Study of Pentosan Polysulfate Sodium and the Development of Pigmentary Maculopathy and Pigmentary Retinopathy
|
||
Completed |
NCT02232282 -
Acupuncture for Female IC/PBSyndrome and Its Effect on the Urinary Microbiome: A Randomized Controlled Trial
|
N/A |