Bladder Instillations Versus Onabotulinumtoxin A for Treatment of Interstitial Cystitis/Bladder Pain Syndrome
A Randomized Trial of Bladder Instillations Versus Onabotulinumtoxin A for Treatment of Interstitial Cystitis/Bladder Pain Syndrome
1 other identifier
interventional
58
1 country
1
Brief Summary
Recognition of interstitial cystitis (IC)/bladder pain syndrome (BPS) is increasing. There is a dire need to develop effective treatment options for these patients as it manifests as more than a physical disease, affecting general and psychological health as well. Existing trials comparing varying bladder instillation formulations have not identified an optimal bladder instillation therapy, however existing studies support combined heparin and alkalinized lidocaine bladder instillation as an affordable and effective treatment for IC/BPS. Additionally, intradetrusor onabotulinumtoxinA injection has been well established for the treatment of overactive bladder (OAB), a constellation of symptoms similar to that of IC/BPS. OnabotulinumtoxinA has now come into the forefront for treatment of OAB due to its efficacy, safety profile, and absence of cognitive effects related to the previous mainstay anticholinergic treatment. While both bladder instillation and onabotulinumtoxinA therapy have been shown to be effective for treatment of IC/BPS, a direct comparison of these treatments has not been performed. We therefore designed a randomized controlled trial to compare the efficacy of heparin with alkalized local anesthetic bladder instillation versus intradetrusor onabotulinumtoxinA injection in treating IC/BPS symptoms.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_2
Started Sep 2020
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 19, 2020
CompletedFirst Posted
Study publicly available on registry
May 26, 2020
CompletedStudy Start
First participant enrolled
September 15, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2023
CompletedOctober 12, 2023
October 1, 2023
2.7 years
May 19, 2020
October 11, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Change in O'Leary-Sant questionnaire scores from baseline between bladder instillation and intradetrusor onabotulinumtoxinA injection groups
Consists of O'Leary-Sant Symptom and Problem Index, total score 0-36.
Baseline, 8-10 weeks
Secondary Outcomes (9)
Change in O'Leary-Sant questionnaire scores from baseline between bladder instillation and intradetrusor onabotulinumtoxinA injection groups
Baseline, 4-6 weeks, 6-9 months
Change in pain scores using the Defense and Veterans Pain Rating Scale (visual analog scale) between bladder instillation and intradetrusor onabotulinumtoxinA injection groups
Baseline, 4-6 weeks, 8-10 weeks, 6-9 months
Change in Female Sexual Function Index (FSFI) score between bladder instillation and intradetrusor onabotulinumtoxinA injection groups
Baseline, 4-6 weeks, 8-10 weeks
Change in Female Sexual Distress Scale-Revised (FSDS-R) score between bladder instillation and intradetrusor onabotulinumtoxinA injection groups
Baseline, 4-6 weeks, 8-10 weeks
Change in 12-item Short Form Survey (SF-12) score between bladder instillation and intradetrusor onabotulinumtoxinA injection groups
Baseline, 4-6 weeks, 8-10 weeks
- +4 more secondary outcomes
Study Arms (2)
Heparin & Alkalinized Lidocaine Bladder Instillation
ACTIVE COMPARATORSix weekly bladder instillations, each instillation consisting of 40,000 IU Heparin, 200mg lidocaine, 2ml 8.4% sodium bicarbonate, sterile water for a total volume 50 milliliters (mL).
Intradetrusor Onabotulinumtoxin A Injection
ACTIVE COMPARATOR100 units onabotulinumtoxinA reconstituted in 10mL of injectable saline, injected in 20 sites with 0.5mL per injection along the posterior wall of the bladder above the trigone.
Interventions
Bladder instillation instilled via catheter and to dwell for minimum of 30 minutes prior to spontaneous void
Intradetrusor onabotulinumtoxinA injection (0.5mL x 20 sites)
Eligibility Criteria
You may qualify if:
- Females ≥ 18 years of age
- O'Leary-Sant questionnaire score ≥ 6
- Ability to follow study instructions and complete all required follow-up
You may not qualify if:
- Contraindications and/or allergies to medications used
- Known alternative diagnosis explaining bladder pain symptoms
- Bladder instillation within the past 3 months
- Intradetrusor onabotulinumtoxinA injection within the past 6 months
- Use of ≥ 400 units of onabotulinumtoxinA in the last 3 months
- Inability or unwillingness to self-catheterize
- Post-void residual \> 200mL
- Concurrent procedural treatment (including hydrodistension, sacral neuromodulation)
- Current use of vaginal pessary/devices
- Untreated symptomatic prolapse \> pelvic organ prolapse quantification system (POP-Q) stage 2
- Females who are pregnant or planning a pregnancy during the study or who think that they may be pregnant at the start of the study and who are unwilling or unable to use a reliable form of contraception during the study
- Inability to speak/read English
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Walter Reed National Military Medical Center
Bethesda, Maryland, 20889, United States
Related Publications (45)
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Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- FED
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 19, 2020
First Posted
May 26, 2020
Study Start
September 15, 2020
Primary Completion
June 1, 2023
Study Completion
June 1, 2023
Last Updated
October 12, 2023
Record last verified: 2023-10