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127 studies found for:    Cystitis, Interstitial
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Rank Status Study
21 Completed Intravesical Liposomes for Ulcerative Cystitis
Condition: Interstitial Cystitis
Intervention: Drug: Liposomes
22 Completed
Has Results
Phase II Study Efficacy and Safety of Two Dosing Regimens of MN-001 in Patients With Interstitial Cystitis
Condition: Interstitial Cystitis
Interventions: Drug: MN-001 BID;   Drug: MN-001;   Drug: Placebo
23 Recruiting Interstitial Cystitis (IC)-Like Findings With Hydrodistension
Condition: Interstitial Cystitis
Interventions: Procedure: Hydrodistension;   Device: Cystoscopy
24 Completed Cyclosporine in Interstitial Cystitis: Efficacy, Safety and Mechanism of Action
Condition: Interstitial Cystitis
Intervention: Drug: Cyclosporine
25 Completed Osteopathic Manipulation Therapy in the Treatment of Interstitial Cystitis
Condition: Interstitial Cystitis
Intervention:
26 Completed Safety Study of LiRIS in Interstitial Cystitis (IC) Patients
Condition: Interstitial Cystitis
Intervention: Drug: LiRIS low dose and LiRIS high dose
27 Recruiting The Efficacy of Biomarker in Patient With Interstitial Cystitis/Painful Bladder Syndrome
Condition: Interstitial Cystitis
Intervention:
28 Unknown  Acupuncture for the Treatment of Interstitial Cystitis (IC) Symptoms
Condition: Interstitial Cystitis
Intervention: Procedure: Acupuncture
29 Enrolling by invitation Autonomic Response During Cystodistension in Patients Suspected of Having Interstitial Cystitis
Condition: Interstitial Cystitis
Intervention:
30 Recruiting Observational Study of Hunner's Ulcer in Patient With Interstitial Cystitis/Bladder Pain Syndrome
Condition: Interstitial Cystitis
Intervention:
31 Completed Safety Study of Single Intravesical Doses of TTI-1612 in Women With Interstitial Cystitis/Bladder Pain Syndrome
Condition: Interstitial Cystitis
Intervention: Drug: TTI-1612
32 Terminated
Has Results
Safety, Tolerability and Efficacy Study of LiRIS® 400 mg in Women With Interstitial Cystitis
Condition: Interstitial Cystitis
Interventions: Drug: LiRIS 400 mg;   Other: LiRIS Placebo
33 Completed Intranasal Ketorolac Tromethamine (Sprix) for Acute Pain of Interstitial Cystitis Flare of Pain
Condition: Interstitial Cystitis
Intervention: Drug: Ketorolac Tromethamine
34 Unknown  Intravesical Instillation of Liposome Encapsulated Botulinum Toxin A (Lipotoxin) in Treatment of Interstitial Cystitis
Condition: Interstitial Cystitis
Interventions: Drug: Liposome encapsulated BoNT-A;   Drug: BOTOX 200U in normal saline;   Drug: Normal saline
35 Terminated
Has Results
Double-Blind Placebo Controlled Study of Safety,Tolerability, and Efficacy of LiRIS® in Women With Interstitial Cystitis
Condition: Interstitial Cystitis
Interventions: Drug: Lidocaine Releasing Intravesical System - LiRIS®;   Other: LiRIS Placebo;   Procedure: Sham Cystoscopy Procedure
36 Recruiting The Efficacy of Additional Intravesical Instillation of Hyaluronic Acid/Chondroitin Sulfate to Transurethral Resection of Bladder Ulcer in Patients With Interstitial Cystitis/Bladder Pain Syndrome.
Condition: Interstitial Cystitis
Intervention: Drug: Hyaluronic acid/chondroitin sulfate
37 Completed
Has Results
A Safety, Tolerability and Preliminary Efficacy Study of LiRIS® 400 mg in Women With Interstitial Cystitis (IC) and Hunner's Lesions
Condition: Chronic Interstitial Cystitis
Intervention: Drug: LiRIS® 400 mg
38 Not yet recruiting A Study to Determine the Role of Toll-like Receptor-4 Expression in Patients With Interstitial Cystitis/Bladder Pain Syndrome
Conditions: Cystitis, Interstitial;   Painful Bladder Syndrome
Intervention: Procedure: cystoscopy, bladder hydrodistention and bladder biopsy
39 Recruiting Evaluation of Intravesical LP08 in Patients With Interstitial Cystitis/Painful Bladder Syndrome
Condition: Interstitial Cystitis
Interventions: Drug: LP-08 80mg;   Drug: Normal Saline Placebo;   Drug: LP-08 20mg
40 Completed Relationship of Interstitial Cystitis to Vulvodynia
Condition: Interstitial Cystitis
Intervention: Other: Physical Examination

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Study has passed its completion date and status has not been verified in more than two years.