Comparing Number of Injection Sites of In-office Intravesical Onabotulinumtoxin A Treatments for Overactive Bladder: A Randomized Controlled Trial
Primary Purpose
Overactive Bladder Syndrome, Overactive Bladder
Status
Not yet recruiting
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
OnabotulinumtoxinA
Sponsored by
About this trial
This is an interventional treatment trial for Overactive Bladder Syndrome
Eligibility Criteria
Inclusion Criteria:
- females, adults 18 years of age and older, diagnosed with OAB
Exclusion Criteria:
- bladder pathology including nephrolithiasis, active urinary tract infection, bladder trauma, neurogenic bladder, patients who have previously received intravesical onabotulinumtoxin A injections, pregnant patients, minor patients, male patients
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Experimental Group
Control Group
Arm Description
100 U of onabotulinumtoxinA toxin diluted in 10 mL of saline cystoscopically injected into approximately 4 different detrusor muscle sites along the posterior bladder wall and dome.
100 U of onabotulinumtoxinA toxin diluted in 10 mL of saline cystoscopically injected into approximately 20 different detrusor muscle sites along the posterior bladder wall and dome.
Outcomes
Primary Outcome Measures
Perceived pain of each participant before, during, and after the procedure on a scale of 0-10
The Pain Survey is a self-reported instrument used to assess pain before, during, and after a procedure. Possible scores range from 0 (no pain) to 10 (worst pain possible).
Secondary Outcome Measures
The Benefit, Satisfaction, and Willingness to Continue of each participant after the procedure
The Benefit, Satisfaction, and Willingness to Continue (BSW) questionnaire is a validated instrument administered by the physician. It asks participants if they had benefit, satisfaction, and a willingness to continue from a specific treatment. If yes, responses range from 1(little benefit, little, satisfaction, a little bit willing) to 2(much benefit, very satisfied, very willing).
Change in extent of Overactive Bladder Symptoms before and after receiving the procedure
The Overactive Bladder questionnaire (OAB-q) short form is a validated instrument that measures the extent to which participants have various symptoms of OAB over the past 4 weeks. The responses range from 1(not at all) to 6(a very great deal).
The Prevalence of complications with botox after receiving the procedure
The Complications with Botox survey is an instrument used to measure if and how many times participants experienced UTIs, difficulty urinating, or hematuria after the Botox procedure. Participants self-report the number of times if they have experienced the side effect.
Full Information
NCT ID
NCT05157295
First Posted
November 23, 2021
Last Updated
December 13, 2021
Sponsor
Augusta University
1. Study Identification
Unique Protocol Identification Number
NCT05157295
Brief Title
Comparing Number of Injection Sites of In-office Intravesical Onabotulinumtoxin A Treatments for Overactive Bladder: A Randomized Controlled Trial
Official Title
Comparing Number of Injection Sites of In-office Intravesical Onabotulinumtoxin A Treatments for Overactive Bladder: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 1, 2022 (Anticipated)
Primary Completion Date
September 30, 2022 (Anticipated)
Study Completion Date
September 30, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Augusta University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
Overactive bladder (OAB) is a syndrome characterized by urinary urgency, with or without urinary incontinence, nocturia, and urinary frequency. Intravesical injection of onabotulinumtoxinA is approved by the US Food and Drug Administration for treatment of neurogenic and idiopathic OAB. Current standard of practice involves 100 U of onabotulinumtoxinA diluted in 10 ml saline cystoscopically injected into approximately 20 different detrusor muscle sites equally distributed along the posterior bladder wall and dome. This treatment was classically done in the operating room under general anesthesia, but now is typically performed in an office setting using local anesthesia (lidocaine) as this is more feasible and tolerable. Patients can experience discomfort and pain with each injection. Evidence has also shown that administering the same dose of onabotulinumtoxinA into fewer injection sites in the detrusor muscle (ranging from 3 to 10) results in equivalent efficacy compared to the current standard. However, it has yet to be determined if there is a significant difference in patient satisfaction and tolerability when the procedure is administered in an office setting using the same dosage with fewer injections. Our study aims to assess whether patient tolerance and satisfaction of intravesicular onabotulinumtoxinA increases with the use of 4 detrusor injections as opposed to 20 injections when performed in an office setting on women with OAB.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overactive Bladder Syndrome, Overactive Bladder
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
One group of participants will receive the "experimental" treatment, which is 4 injections, and the other group of participants will receive the "standard" treatment, which is 20 injections.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental Group
Arm Type
Experimental
Arm Description
100 U of onabotulinumtoxinA toxin diluted in 10 mL of saline cystoscopically injected into approximately 4 different detrusor muscle sites along the posterior bladder wall and dome.
Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
100 U of onabotulinumtoxinA toxin diluted in 10 mL of saline cystoscopically injected into approximately 20 different detrusor muscle sites along the posterior bladder wall and dome.
Intervention Type
Drug
Intervention Name(s)
OnabotulinumtoxinA
Intervention Description
100 U of Onabotulinumtoxin A diluted in 10 mL of saline injected into the wall of the detrusor muscle at various sites
Primary Outcome Measure Information:
Title
Perceived pain of each participant before, during, and after the procedure on a scale of 0-10
Description
The Pain Survey is a self-reported instrument used to assess pain before, during, and after a procedure. Possible scores range from 0 (no pain) to 10 (worst pain possible).
Time Frame
within the hour prior to initiating the intervention, and immediately at the conclusion of the 30-minute intervention
Secondary Outcome Measure Information:
Title
The Benefit, Satisfaction, and Willingness to Continue of each participant after the procedure
Description
The Benefit, Satisfaction, and Willingness to Continue (BSW) questionnaire is a validated instrument administered by the physician. It asks participants if they had benefit, satisfaction, and a willingness to continue from a specific treatment. If yes, responses range from 1(little benefit, little, satisfaction, a little bit willing) to 2(much benefit, very satisfied, very willing).
Time Frame
2 weeks +/- 7 days after procedure and 3 +/- 7 days months after procedure
Title
Change in extent of Overactive Bladder Symptoms before and after receiving the procedure
Description
The Overactive Bladder questionnaire (OAB-q) short form is a validated instrument that measures the extent to which participants have various symptoms of OAB over the past 4 weeks. The responses range from 1(not at all) to 6(a very great deal).
Time Frame
Pre procedure, 2 weeks +/- 7 days after procedure, and 3 +/- 7 days months after procedure
Title
The Prevalence of complications with botox after receiving the procedure
Description
The Complications with Botox survey is an instrument used to measure if and how many times participants experienced UTIs, difficulty urinating, or hematuria after the Botox procedure. Participants self-report the number of times if they have experienced the side effect.
Time Frame
2 weeks +/- 7 days after procedure, and 3 +/- 7 days months after procedure
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
females, adults 18 years of age and older, diagnosed with OAB
Exclusion Criteria:
bladder pathology including nephrolithiasis, active urinary tract infection, bladder trauma, neurogenic bladder, patients who have previously received intravesical onabotulinumtoxin A injections, pregnant patients, minor patients, male patients
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stacy Carrigan
Phone
7067214959
Email
scarrigan@augusta.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer Lanzer, MD
Organizational Affiliation
Augusta University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Emily Grandprey, DO
Organizational Affiliation
Augusta University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Emily Lluch
Organizational Affiliation
Augusta University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ahana Gaurav
Organizational Affiliation
Augusta University
Official's Role
Study Director
12. IPD Sharing Statement
Plan to Share IPD
No
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Comparing Number of Injection Sites of In-office Intravesical Onabotulinumtoxin A Treatments for Overactive Bladder: A Randomized Controlled Trial
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