Intravesical Liposomes for Interstitial Cystitis/Painful Bladder Syndrome (IC/PBS)

Not Applicable

Completed

• Conditions: Interstitial Cystitis; Pelvic Pain
• Interventions: Biological: Liposomes

• Registration Number: NCT01731470
• Lead Sponsor: Kenneth Peters, MD

Brief Summary

Interstitial cystitis/painful bladder syndrome (IC/PBS) is a poorly understood chronic disorder of unknown etiology consisting of irritative bladder symptoms and pelvic pain that dramatically affects quality of life.

Preclinical study data (obtained by using an IC/PBS model in Sprague-Dawley female rats) have demonstrated normalization of urinary frequency indicating that LP may be a potent protectant of the bladder mucosa against inflammation and irritation. Intravesical LP has so far demonstrated an excellent safety profile and minimal toxicity at concentrations of 2 mg/ml. Thus, we hypothesize that intravesical instillation of LP may form a molecular film on bladder ulcer surfaces in patients with IC and provide a safe, effective, and minimally invasive treatment option to alleviating symptoms.

Detailed Description

Liposomes (LP), the treatment article in this proposal, were discovered in the process of exploring a "control" compound when measuring the efficacy of liposomally encapsulated capsaicin for the intravesical treatment of interstitial cystitis. Liposomes are lipid vesicles composed of concentric phospholipid bilayers, which enclose an aqueous interior. Liposomes have the ability to form a molecular film on cell and tissue surfaces and are currently being tested as possible therapeutic agents to promote wound healing. Application of liposomes at the wound surface provides a moist protective film over the wound and augments wound healing without chronic inflammatory reactions in the neodermal layer.

Study Timeline

• Study Start: 2012-07
• Study First Submitted: 2012-11-15
• Study First Submitted QC: 2012-11-15
• Study First Posted: 2012-11-21
• Primary Completion: 2013-08
• Study Completion: 2013-08
• Results First Submitted: 2016-05-12
• Status Verified: 2016-11
• Results First Submitted QC: 2016-11-13
• Last Update Submitted: 2016-11-13
• Results First Posted: 2017-01-10
• Last Update Posted: 2017-01-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 14

Inclusion Criteria

• • Written informed consent has been obtained

  • Males and females, at least 18 years of age
  • History of IC/PBS for at least 6 months documented in the medical record
  • Recurring IC/PBS symptoms
  • An average of 8 or more urine voids over a 3-day period, confirmed by the baseline voiding diary
  • Bladder pain score > 4 in the last 24 hours (assessed at screening visit)
  • Previous use of medications and/or treatment(s) for symptom relief
  • Females of child-bearing capability agree to use a reliable form of birth control (condoms and/or oral contraceptives (birth control pills)) during the 4 week course of therapy and 1 week thereafter
  • Willing and capable of understanding and complying with all requirements of the protocol, including proper completion of the voiding diaries and self-administered questionnaires

Exclusion Criteria

• • Subjects currently taking prescribed medications for IC/PBS will be able to continue the medications throughout the course of the study. If the patient cannot be maintained on a stable dose of the medication(s) throughout the treatment and follow-up period they will be excluded.

  • Subjects must not have had intravesical treatment(s)/bladder installations of the following medications: dimethylsulfoxide (DMSO), lidocaine and/or heparin within 1 month prior to study visit 1
  • Pregnant or lactating
  • History of bleeding diathesis
  • Currently on anticoagulant therapy (e.g. warfarin, clopidogrel)
  • Active bleeding peptic ulcer disease
  • Obvious neurological impairment which may be affecting bladder function
  • Known allergy to liposomes and/or egg yolk
  • Current or previous participation in another therapeutic or device study within 6 months of the screening visit
  • The presence of any clinically significant systemic disease or condition that in the opinion of the investigator would make the patient unsuitable for the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Liposomes	Liposomes	Liposomes

Primary Outcome Measures

Name	Time	Method
Change in Symptom Severity at 4 and 8 Weeks Post-Treatment as Measured by the Total O'Leary-Sant IC Symptom and Problem Index (ICSI/ICPI) Score	4 and 8 weeks post-treatment	The O'Leary-Sant IC Symptom Index (ICS-I) total score ranges from 0 to 20 and the Problem Index (ICP-I) total score ranges from 0 to 16. Each index has 4 questions and lower scores represent a better outcome. A total ICSI/ICPI score is obtained by adding the total scores from both indices. The combined ICSI/ICPI total score ranges from 0 to 36.

Secondary Outcome Measures

Name	Time	Method
Change in Pain Scores at 4 and 8 Weeks Post-Treatment as Measured by the Visual Analog Scale (VAS)	4 and 8 weeks post-treatment	Patients utilized the Visual Analog Scale (VAS) to describe their pain. The scale ranges from 0:No pain to 10: Pain as bad as it could possibly be.

Trial Locations

Locations (1)

William Beaumont Hospital; 🇺🇸 Royal Oak, Michigan, United States