Urodynamic Changes Following Fewer Injection Sites of Intravesical Botulinum Toxin in Idiopathic Detrusor Overactivity: A Double-Blinded Prospective Randomized Clinical Trial

Soleimanifard N1, Emami M2, Moghimian M2, Kaffash Nayeri R2, Tayebi S2

Research Type

Clinical

Abstract Category

Overactive Bladder

Abstract 133
Urology 5 - Lower Urinary Tract Symptoms Therapy
Scientific Podium Short Oral Session 12
Friday 19th September 2025
09:00 - 09:07
Parallel Hall 3
Clinical Trial Detrusor Overactivity Overactive Bladder Urgency Urinary Incontinence Urgency/Frequency
1. Shahid Labbafinejad Medical Center, The Center of Excellence in Urology, Shahid Beheshti University of Medical Sciences, Tehran, Iran, 2. Department of Urology, Hasheminejad Kidney Center, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
Presenter
Links

Abstract

Hypothesis / aims of study
‏This study aimed to evaluate the efficacy of a modified intravesical botulinum toxin injection technique with fewer injection sites under local anesthesia compared to the conventional method in patients with idiopathic detrusor overactivity, focusing on urodynamic outcomes.
Study design, materials and methods
‏In this double-blinded randomized clinical trial, 78 adult female patients with idiopathic detrusor overactivity were divided into two groups. The conventional group received 20-site intradetrusor botulinum toxin injections under general or spinal anesthesia, while the modified group received five injections beyond the trigone under local anesthesia. The primary outcome was the comparison of urodynamic parameters between the groups, and the secondary outcomes included safety and tolerability assessments.
Results
‏Baseline urodynamic parameters showed no significant differences between the groups. Post-intervention, both methods demonstrated significant improvements in bladder capacity, detrusor pressure, and overactivity episodes, with no statistically significant differences between the two groups. The modified technique was well tolerated without the need for conversion to general anesthesia. Adverse events were minimal and comparable between groups.
Interpretation of results
Our study demonstrated that reducing the number of botulinum toxin injection sites from 20 to 5, while using local anesthesia, results in similar improvements in urodynamic parameters compared to the conventional method. Significant increases in bladder capacity and reductions in detrusor pressure and overactivity episodes were observed in both groups, with no significant differences between them. Additionally, the modified technique was well tolerated by all patients without the need for conversion to general anesthesia, highlighting its feasibility for outpatient settings. This approach may provide a less invasive and more accessible alternative for treating idiopathic detrusor overactivity while maintaining efficacy and safety
Concluding message
‏Reducing the number of botulinum toxin injection sites while using local anesthesia is as effective as the conventional method for improving urodynamic outcomes in patients with idiopathic detrusor overactivity. This approach offers a well-tolerated, feasible alternative that may be performed in an outpatient setting, minimizing the need for general anesthesia.
References
  1. Abrams P, Andersson K-E, Birder L, Brubaker L, Cardozo L, Chapple C, et al. Fourth international consultation on incontinence recommendations of the international scientific committee: evalu- ation and treatment of urinary incontinence, pelvic organ prolapse, and fecal incontinence. Neurourol Urodyn. 2010;29(1):213–40.
  2. Chen JL, Kuo HC. Clinical application of intravesical botulinum toxin type A for overactive bladder and interstitial cystitis. Investig Clin Urol. 2020;61(Suppl 1):S33–42.
  3. Apostolidis A, Papaefstathiou E, Gatsos S. Intravesical Botox for overactive bladder: how to minimize complications and manage failures. Curr Drug Targets. 2020;21(15):1527–36.
Disclosures
Funding This study was funded by the Research Vice Chancellor of Iran University of Medical Sciences. Clinical Trial Yes Registration Number Iranian Registry of Clinical Trials (IRCT) Registration Number: IRCT20210214050354N1 RCT Yes Subjects Human Ethics Committee ethics committee of Iran University of Medical Sciences, Tehran, Iran (ethics code IRCT20210214050354N1) Helsinki Yes Informed Consent Yes
08/07/2025 10:00:34