NCT04401176

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
58

participants targeted

Target at P25-P50 for phase_2

Timeline
Completed

Started Sep 2020

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 19, 2020

Completed
7 days until next milestone

First Posted

Study publicly available on registry

May 26, 2020

Completed
4 months until next milestone

Study Start

First participant enrolled

September 15, 2020

Completed
2.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2023

Completed
Last Updated

October 12, 2023

Status Verified

October 1, 2023

Enrollment Period

2.7 years

First QC Date

May 19, 2020

Last Update Submit

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 COMPARATOR

Six 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).

Drug: Heparin & Alkalinized Lidocaine Bladder Instillation

Intradetrusor Onabotulinumtoxin A Injection

ACTIVE COMPARATOR

100 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.

Drug: Onabotulinum Toxin A

Interventions

Bladder instillation instilled via catheter and to dwell for minimum of 30 minutes prior to spontaneous void

Heparin & Alkalinized Lidocaine Bladder Instillation

Intradetrusor onabotulinumtoxinA injection (0.5mL x 20 sites)

Intradetrusor Onabotulinumtoxin A Injection

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

Related Publications (45)

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    PMID: 30917614BACKGROUND
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    PMID: 22278835BACKGROUND
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    PMID: 24568045BACKGROUND
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    PMID: 12913705BACKGROUND
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    PMID: 11432309BACKGROUND
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Related Links

MeSH Terms

Conditions

Cystitis, Interstitial

Interventions

Heparinonabotulinum toxin A

Condition Hierarchy (Ancestors)

CystitisUrinary Bladder DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital Diseases

Intervention Hierarchy (Ancestors)

GlycosaminoglycansPolysaccharidesCarbohydrates

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

Locations