Amniotic Membrane Therapy for Interstitial Cystitis/Painful Bladder Syndrome

Interstitial Cystitis Clinical Trial

Official title:

Amniotic Membrane Therapy for Interstitial Cystitis/Painful Bladder Syndrome (IC/PBS): a Prospective, Double-Blind, Randomized Controlled Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06096597
• Other study ID #: STUDY20231301
• Status: Not yet recruiting
• Phase: Phase 2/Phase 3
• Start date: July 2024
• Est. completion date: June 2026

Study information

• Verified date: May 2024
• Source: University Hospitals Cleveland Medical Center
• Contact: Margot Le Neveu, MD
• Phone: ?(440) 895-7685
• Email: Margot.LeNeveu[@]uhhospitals.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Interstitial cystitis/painful bladder syndrome (IC/PBS) is a clinical syndrome in which patients report symptoms of bladder and/or pelvic pain with pressure and/ or discomfort associated with urinary frequency and urgency.

The primary objective of this study is to determine the efficacy of amniotic membrane therapy in patients with interstitial cystitis/painful bladder syndrome (IC/PBS) as defined by clinically-significant improvement in validated symptom questionnaires.

Description:

Interstitial cystitis/painful bladder syndrome (IC/PBS) is a clinical syndrome in which patients report symptoms of bladder and/or pelvic pain with pressure and/or discomfort associated with urinary frequency and urgency. These symptoms vary in severity and are known to cause significant impact on quality of life. Current recommended therapies include behavior modifications, stress management practices, physical therapy, oral pharmacologic pain management agents, intravesical instillations, hydrodistension, fulguration of bladder lesions and/or triamcinolone injections, intradetrusor onabotulinumtoxin A injections, neuromodulation, and major surgery.

Amniotic membranes, Clarix FLO™, have been used to assist in wound healing in many fields of medicine, and its use has evolved over the last century to various applications in regenerative medicine. A novel study using amniotic membranes for bladder therapy has showing promising preliminary results in a small cohort study of 10 females with recalcitrant IC/PBS. These women underwent intradetrusor injections of micronized amniotic membranes and had significant improvement of voiding symptoms and bladder pain over 3 months with no adverse events. No randomized controlled trials (RCT) of amniotic bladder therapy have been conducted to date. The proposed study would be the first RCT assessing the efficacy of amniotic membrane injections with Clarix FLO™ and has the potential to make significant impacts in the management and treatment of patients with IC/PBS.

Clarix FLO™ is a sterile, particulate human amniotic membrane and umbilical cord tissue product that is aseptically processed in compliance with current Good Tissue Practices from the same donated human tissue (placenta) after determination of eligibility and placenta/cord suitability. Amniotic Membrane and Umbilical Cord products are currently designated by the FDA as tissue products under PHS Act 361 HCT/P (human cells, tissues and cellular and tissue-based products). Clarix FLO™ does not contain living cells.

Patients will then be followed with clinical evaluation and questionnaires repeated at 2, 4, 8 and 12 weeks post-operatively. Additional urine culture and post void residuals will be repeated at 2 and 4 weeks post-operatively. Primary Objective: Determine the efficacy of amniotic bladder therapy (ABT) in patients with interstitial cystitis/painful bladder syndrome (IC/PBS) as defined by clinically-significant improvement

• Clinically-meaningful indicator defined as: 5 point reduction in Interstitial Cystitis Symptom Index (ICSI)

Secondary Objectives:

• Characterize duration of effect of ABT using clinical evaluation and the following questionnaires:

• Interstitial Cystitis Symptom Index (ICSI)

• Interstitial Cystitis Problem Index (ICPI)

• Bladder Pain/Interstitial Cystitis Symptom Score (BPIC-SS)

• Overactive Bladder Assessment Tool

• PUF

• SF-12 Health Survey

• Determine if there are any adverse effects of ABT, such as urinary tract infections or acute urinary retention.

Hypothesis: ABT in patients with PBS improves clinical outcomes

Other known NCT identifiers

• NCT06104787

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Est. completion date: June 2026
• Est. primary completion date: June 2026
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients 18 years of age or older

• Female

• English Speaking

• Diagnosis of IC/PBS

• Have failed at least one prior treatment for IC/PBS

Exclusion Criteria:

• Patients less than 18 years of age

• Unable to provide consent

• Non-English speaking

• Patients with known anatomical malformations of the ureters, bladder, or urethra

Related Conditions & MeSH terms

• Cystitis
• Cystitis, Interstitial
• Interstitial Cystitis
• Pain
• Painful Bladder Syndrome
• Painful Bladder Syndrome (PBS)
• Syndrome

Intervention

Drug:
• Clarix Flo
100 mg of commercially available micronized amniotic membrane (Clarix Flo; BioTissue, Miami, FL) diluted in 10 mL of 0.9% preservative-free sodium chloride
• Placebo
10 mL of 0.9% preservative-free sodium chloride

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
David Sheyn

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Interstitial Cystitis Symptom Index (ICSI) score	Evaluate for clinically-meaningful reduction in symptoms as defined as a 5 point reduction in Interstitial Cystitis Symptom Index (ICSI)	To be completed pre-operatively and at 2, 4, 8 and 12 weeks post-operatively
Secondary	Change in Interstitial Cystitis Symptom Index Questionnaire	To determine the change in interstitial cystitis symptoms in participants who received amniotic membrane injection versus placebo injection (saline) as measured using the Interstitial Cystitis Symptom Index (ICSI).	To be completed pre-operatively and at 2, 4, 8 and 12 weeks post-operatively
Secondary	Change in Interstitial Cystitis Problem Index Questionnaire	To determine the change in interstitial cystitis symptoms in participants who received amniotic membrane injection versus placebo injection (saline) as measured using the Interstitial Cystitis Problem Index (ICPI).	To be completed pre-operatively and at 2, 4, 8 and 12 weeks post-operatively
Secondary	Change in Bladder Pain/ Interstitial Cystitis Symptom Score	To determine the change in interstitial cystitis symptoms in participants who received amniotic membrane injection versus placebo injection (saline) as measured using the Bladder Pain/Interstitial Cystitis Symptom Score (BPIC-SS).	To be completed pre-operatively and at 2, 4, 8 and 12 weeks post-operatively
Secondary	Change in Overactive Bladder Assessment Tool Scores	To determine the change in interstitial cystitis symptoms in participants who received amniotic membrane injection versus placebo injection (saline) as measured using the Overactive Bladder Assessment Tool	To be completed pre-operatively and at 2, 4, 8 and 12 weeks post-operatively
Secondary	Change in SF-12 Health Survey Scores	To determine the change in interstitial cystitis symptoms in participants who received amniotic membrane injection versus placebo injection (saline) as measured using the SF-12 Health Survey	To be completed pre-operatively and at 2, 4, 8 and 12 weeks post-operatively
Secondary	Change in Pelvic Pain and Urgency/ Frequency (PUF) Patient Symptom Scale (PUF) Scores	To determine the change in interstitial cystitis symptoms in participants who received amniotic membrane injection versus placebo injection (saline) as measured using the PUF Questionnaire	To be completed pre-operatively and at 2, 4, 8 and 12 weeks post-operatively
Secondary	Change in number of urinary tract infections as measured by medical record review	As defined by symptoms of urinary tract infection and positive urine culture	To be completed pre-operatively and at 2, 4, 8 and 12 weeks post-operatively