Intradetrusor Botulinum Toxin A: Are Less Injections Better?
Primary Purpose
Overactive Bladder, Urinary Urge Incontinence, Overactive Bladder Syndrome
Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
OnabotulinumtoxinA 100 UNT [Botox]
Sponsored by
About this trial
This is an interventional treatment trial for Overactive Bladder
Eligibility Criteria
Inclusion Criteria:
- Female
- 18 years old or greater
- Diagnosis of overactive bladder (urinary urgency or frequency, OAB) or urinary urgency incontinence (UUI)
Exclusion Criteria:
- Have a diagnosis of neurogenic bladder
- Received intravesical botox injections within prior 6 months
- Current treatment with either: SNM, PTNS, or OAB medications - need wash out as below
- SNM - turn device off for at least 2 weeks prior to procedure, off during 3-month follow up window
- PTNS - no treatments within 2 weeks of start, none during 3-month post-procedure follow up window
- OAB meds - 2 week wash out period prior to injection, none during 3-month post-procedure follow up window
- Currently pregnant or trying to get pregnant
- Contraindications to Botox® - hypersensitivity to Botox®, inability to self-catheterize/refusal to have indwelling catheter
- Have a UTI (can enroll after treatment)
- Have urinary retention (PVR>150cc on two occasions)
- Do not speak English or Spanish
Sites / Locations
- University of California Irvine Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
1 Injection Site
10 Injection Sites
Arm Description
100u Botox® injected at one intradetrusor site
100u Botox® injected at 10 intradetrusor sites
Outcomes
Primary Outcome Measures
Change in Overactive Bladder Questionnaire Long Form Score (symptoms severity sub-scale)(OAB-Q LF)
Participants will be asked to Overactive Bladder Questionnaire Long Form prior to receiving the Botox procedure. The OAB-Q LF symptom severity sub-scale score will be compared prior to procedure and again to score at 3 weeks after procedure.
The OAB-q Symptom Severity Score will be computed at baseline and 3 weeks (and 3 months) using the standard scoring algorithm. Minimum value of symptom severity subscale is 8, maximum is 48. A higher score means worse symptoms. A lower score means less symptoms.
Secondary Outcome Measures
Change in Overactive Bladder Questionnaire Long Form Score (symptoms severity sub-scale)(OAB-Q LF)
Participants will be asked to complete Overactive Bladder Questionnaire Long Form prior to receiving the Botox procedure. The OAB-Q LF symptom severity sub-scale score will be compared prior to procedure and again to score at 3 months after procedure.
The OAB-q Symptom Severity Score will be computed at baseline and 3 weeks (and 3 months) using the standard scoring algorithm. Minimum value of symptom severity subscale is 8, maximum is 48. A higher score means worse symptoms. A lower score means less symptoms.
Post-void residual (PVR)
A PVR will be collected via either urethral catheterization or bladder scan (ultrasound in clinic) at 3 weeks post-procedure as a marker of urinary retention. The PVRs will be compared between study and control groups
Number of participants with urinary tract infection (UTI)
Urine culture will be sent for any patient with urinary tract infections symptoms (eg: worsening urgency, frequency, dysuria).
Patient Global Impression - Improvement (PGI-I)
Participants will complete PGI-I Questionnaire at 3 months after procedure. The minimum value is 1 (very much better) and maximum value score is 7 (very much worse). A higher score indicates worse symptoms. A lower score indicates better symptoms or more improvement.
Visual Analogue Scale (VAS) - Pain
Participants will complete VAS-pain immediately post-procedure as a pain and tolerability assessment
Full Information
NCT ID
NCT05308979
First Posted
March 15, 2022
Last Updated
July 18, 2023
Sponsor
University of California, Irvine
Collaborators
Kaiser Permanente, St. Joseph Hospital of Orange
1. Study Identification
Unique Protocol Identification Number
NCT05308979
Brief Title
Intradetrusor Botulinum Toxin A: Are Less Injections Better?
Official Title
Intradetrusor Botulinum Toxin A: Can Less Injections Maintain Efficacy and Improve Patient Satisfaction?
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2022 (Actual)
Primary Completion Date
October 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Irvine
Collaborators
Kaiser Permanente, St. Joseph Hospital of Orange
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
Yes
5. Study Description
Brief Summary
Patients with either overactive bladder (OAB) or urgency urinary incontinence (UUI) with be randomized (like a flip of a coin) to receive 100 units of bladder Botox® at either one injection site or ten injection sites. Efficacy and patient satisfaction will be measured by questionnaires.
Detailed Description
Intradetrusor (bladder) Botulinum toxin A (BTA or Botox®) is a well-established treatment for urinary urgency incontinence (UUI).[1,2] While this treatment's efficacy in comparison to alternative therapies including anticholinergic medications and sacral neuromodulation for treatment of UUI has been studied, the ideal number of injection sites within the bladder has not been well established. [3,4] Intradetrusor BTA injections are often completed as an office procedure while the patient is awake. Each injection site can cause discomfort for the patient during the procedure. Urinary tract infection and urinary retention are risks associated with this procedure and could potentially be related to number of injection sites. Currently, there is a lack of information in the literature regarding the optimal number of intravesical BTA injection sites.
Prior studies evaluated efficacy using 100u BTA spread across 20 injections sites, however current practices at local institutions safely use 10 injections sites based on studies showing similar effect and adverse event profiles between use of 10, 20, and 40 injection sites.[5,6] Research using animal models has shown diffuse distribution of BTA within the entire detrusor muscle after just a single BTA injection at one site.[7] This has been corroborated in human studies.[8] A recently published observational pilot study shows promise for single site intradetrusor Botox® injection as it reported a lower rate of urinary retention and similar durability.[9] Similar clinical efficacy with only one to three intravesical BTA injection[s] has also been reported.[10]
In this study, participants will be randomized to receive 100u BTA via intradetrusor injection at one injection site (experimental) versus 10 injection sites (control). Investigators hypothesize that one injection will have similar efficacy to multiple injections and potentially better tolerability and patient satisfaction, due to decreased procedure time and less pain, along with potential for lower adverse event rates, specifically urinary retention and urinary tract infections.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overactive Bladder, Urinary Urge Incontinence, Overactive Bladder Syndrome, Urinary Incontinence, Urge, Urge Incontinence, Urinary Urgency, Urinary Frequency
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Parallel study with 2 arms, 1:1 randomization
Masking
Participant
Allocation
Randomized
Enrollment
102 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
1 Injection Site
Arm Type
Experimental
Arm Description
100u Botox® injected at one intradetrusor site
Arm Title
10 Injection Sites
Arm Type
Active Comparator
Arm Description
100u Botox® injected at 10 intradetrusor sites
Intervention Type
Drug
Intervention Name(s)
OnabotulinumtoxinA 100 UNT [Botox]
Intervention Description
Intradetrusor (Bladder) Botox Injection at 1 vs 10 injection sites
Primary Outcome Measure Information:
Title
Change in Overactive Bladder Questionnaire Long Form Score (symptoms severity sub-scale)(OAB-Q LF)
Description
Participants will be asked to Overactive Bladder Questionnaire Long Form prior to receiving the Botox procedure. The OAB-Q LF symptom severity sub-scale score will be compared prior to procedure and again to score at 3 weeks after procedure.
The OAB-q Symptom Severity Score will be computed at baseline and 3 weeks (and 3 months) using the standard scoring algorithm. Minimum value of symptom severity subscale is 8, maximum is 48. A higher score means worse symptoms. A lower score means less symptoms.
Time Frame
change from baseline OAB-Q score to 3 wk post-procedure score
Secondary Outcome Measure Information:
Title
Change in Overactive Bladder Questionnaire Long Form Score (symptoms severity sub-scale)(OAB-Q LF)
Description
Participants will be asked to complete Overactive Bladder Questionnaire Long Form prior to receiving the Botox procedure. The OAB-Q LF symptom severity sub-scale score will be compared prior to procedure and again to score at 3 months after procedure.
The OAB-q Symptom Severity Score will be computed at baseline and 3 weeks (and 3 months) using the standard scoring algorithm. Minimum value of symptom severity subscale is 8, maximum is 48. A higher score means worse symptoms. A lower score means less symptoms.
Time Frame
comparison of baseline OAB-Q score to 3 month post-procedure score
Title
Post-void residual (PVR)
Description
A PVR will be collected via either urethral catheterization or bladder scan (ultrasound in clinic) at 3 weeks post-procedure as a marker of urinary retention. The PVRs will be compared between study and control groups
Time Frame
PVR collected at 3 wk post-procedure
Title
Number of participants with urinary tract infection (UTI)
Description
Urine culture will be sent for any patient with urinary tract infections symptoms (eg: worsening urgency, frequency, dysuria).
Time Frame
anytime after procedure, until at least 3 months post-procedure.
Title
Patient Global Impression - Improvement (PGI-I)
Description
Participants will complete PGI-I Questionnaire at 3 months after procedure. The minimum value is 1 (very much better) and maximum value score is 7 (very much worse). A higher score indicates worse symptoms. A lower score indicates better symptoms or more improvement.
Time Frame
3 months after botox procedure
Title
Visual Analogue Scale (VAS) - Pain
Description
Participants will complete VAS-pain immediately post-procedure as a pain and tolerability assessment
Time Frame
immediately after procedure
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Female
18 years old or greater
Diagnosis of overactive bladder (urinary urgency or frequency, OAB) or urinary urgency incontinence (UUI)
Exclusion Criteria:
Have a diagnosis of neurogenic bladder
Received intravesical botox injections within prior 6 months
Current treatment with either: SNM, PTNS, or OAB medications - need wash out as below
SNM - turn device off for at least 2 weeks prior to procedure, off during 3-month follow up window
PTNS - no treatments within 2 weeks of start, none during 3-month post-procedure follow up window
OAB meds - 2 week wash out period prior to injection, none during 3-month post-procedure follow up window
Currently pregnant or trying to get pregnant
Contraindications to Botox® - hypersensitivity to Botox®, inability to self-catheterize/refusal to have indwelling catheter
Have a UTI (can enroll after treatment)
Have urinary retention (PVR>150cc on two occasions)
Do not speak English or Spanish
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carly Crowder, MD
Phone
714-456-2911
Email
crowderc@hs.uci.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Taylor Brueseke, MD
Phone
714-456-2911
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carly Crowder, MD
Organizational Affiliation
UC Irvine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Taylor Brueseke, MD
Organizational Affiliation
UC Irvine
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Felicia Lane, MD
Organizational Affiliation
UC Irvine
Official's Role
Study Chair
Facility Information:
Facility Name
University of California Irvine Medical Center
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carly Crowder
Phone
714-456-2911
First Name & Middle Initial & Last Name & Degree
Taylor Brueseke, MD
First Name & Middle Initial & Last Name & Degree
Felicia Lane, MD
First Name & Middle Initial & Last Name & Degree
Dena Moskowitz, MD
First Name & Middle Initial & Last Name & Degree
Afiba Arthur, MD
First Name & Middle Initial & Last Name & Degree
Brittni Boyd, MD
First Name & Middle Initial & Last Name & Degree
Emily Whitcomb, MD
First Name & Middle Initial & Last Name & Degree
Noelani Guaderrama, MD
First Name & Middle Initial & Last Name & Degree
Jennifer Lee, MD
First Name & Middle Initial & Last Name & Degree
Carly Crowder, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
18499184
Citation
Brubaker L, Richter HE, Visco A, Mahajan S, Nygaard I, Braun TM, Barber MD, Menefee S, Schaffer J, Weber AM, Wei J; Pelvic Floor Disorders Network. Refractory idiopathic urge urinary incontinence and botulinum A injection. J Urol. 2008 Jul;180(1):217-22. doi: 10.1016/j.juro.2008.03.028. Epub 2008 May 21.
Results Reference
background
PubMed Identifier
23608668
Citation
Chapple C, Sievert KD, MacDiarmid S, Khullar V, Radziszewski P, Nardo C, Thompson C, Zhou J, Haag-Molkenteller C. OnabotulinumtoxinA 100 U significantly improves all idiopathic overactive bladder symptoms and quality of life in patients with overactive bladder and urinary incontinence: a randomised, double-blind, placebo-controlled trial. Eur Urol. 2013 Aug;64(2):249-56. doi: 10.1016/j.eururo.2013.04.001. Epub 2013 Apr 10.
Results Reference
background
PubMed Identifier
23036134
Citation
Visco AG, Brubaker L, Richter HE, Nygaard I, Paraiso MF, Menefee SA, Schaffer J, Lowder J, Khandwala S, Sirls L, Spino C, Nolen TL, Wallace D, Meikle SF; Pelvic Floor Disorders Network. Anticholinergic therapy vs. onabotulinumtoxina for urgency urinary incontinence. N Engl J Med. 2012 Nov 8;367(19):1803-13. doi: 10.1056/NEJMoa1208872. Epub 2012 Oct 4.
Results Reference
background
PubMed Identifier
27701661
Citation
Amundsen CL, Richter HE, Menefee SA, Komesu YM, Arya LA, Gregory WT, Myers DL, Zyczynski HM, Vasavada S, Nolen TL, Wallace D, Meikle SF. OnabotulinumtoxinA vs Sacral Neuromodulation on Refractory Urgency Urinary Incontinence in Women: A Randomized Clinical Trial. JAMA. 2016 Oct 4;316(13):1366-1374. doi: 10.1001/jama.2016.14617.
Results Reference
background
PubMed Identifier
23246476
Citation
Nitti VW, Dmochowski R, Herschorn S, Sand P, Thompson C, Nardo C, Yan X, Haag-Molkenteller C; EMBARK Study Group. OnabotulinumtoxinA for the treatment of patients with overactive bladder and urinary incontinence: results of a phase 3, randomized, placebo controlled trial. J Urol. 2013 Jun;189(6):2186-93. doi: 10.1016/j.juro.2012.12.022. Epub 2012 Dec 14.
Results Reference
background
PubMed Identifier
25914349
Citation
Liao CH, Chen SF, Kuo HC. Different number of intravesical onabotulinumtoxinA injections for patients with refractory detrusor overactivity do not affect treatment outcome: A prospective randomized comparative study. Neurourol Urodyn. 2016 Aug;35(6):717-23. doi: 10.1002/nau.22780. Epub 2015 Apr 24.
Results Reference
background
PubMed Identifier
22306320
Citation
Coelho A, Cruz F, Cruz CD, Avelino A. Spread of onabotulinumtoxinA after bladder injection. Experimental study using the distribution of cleaved SNAP-25 as the marker of the toxin action. Eur Urol. 2012 Jun;61(6):1178-84. doi: 10.1016/j.eururo.2012.01.046. Epub 2012 Feb 1.
Results Reference
background
PubMed Identifier
19145439
Citation
Mehnert U, Boy S, Schmid M, Reitz A, von Hessling A, Hodler J, Schurch B. A morphological evaluation of botulinum neurotoxin A injections into the detrusor muscle using magnetic resonance imaging. World J Urol. 2009 Jun;27(3):397-403. doi: 10.1007/s00345-008-0362-0. Epub 2009 Jan 15.
Results Reference
background
PubMed Identifier
33742316
Citation
Ton J, Downing P, Versi E, van Uem S, Ephraim S, Murphy M, Lucente V. Outcomes of a single trigone-only vs. 20 trigone-sparing injections of OnabotulinumtoxinA for refractory overactive bladder (OAB). Int Urol Nephrol. 2021 Jun;53(6):1067-1072. doi: 10.1007/s11255-021-02802-0. Epub 2021 Mar 19.
Results Reference
background
PubMed Identifier
27283922
Citation
Avallone MA, Sack BS, El-Arabi A, Guralnick ML, O'Connor RC. Less is more-A pilot study evaluating one to three intradetrusor sites for injection of OnabotulinumtoxinA for neurogenic and idiopathic detrusor overactivity. Neurourol Urodyn. 2017 Apr;36(4):1104-1107. doi: 10.1002/nau.23052. Epub 2016 Jun 10.
Results Reference
background
Learn more about this trial
Intradetrusor Botulinum Toxin A: Are Less Injections Better?
We'll reach out to this number within 24 hrs