Lidocaine instillation versus no analgesia in patients undergoing outpatient intravesical OnabotulinumtoxinA-injections: the STILL study, a prospective multi-center study

Adema G1, Heijgele K1, Ploumen E1, Koldewijn E2, Fransen M2, Hobijn M3, Smits M4, Rademakers K1, Bruins M1

Research Type

Clinical

Abstract Category

Overactive Bladder

Abstract 207
Female LUTS, SUI and Imaging 2
Scientific Podium Short Oral Session 24
Friday 9th October 2026
09:15 - 09:22
Parallel Hall 3
0.4 Brussels / 0.5 Paris
Capacity: 356
Overactive Bladder Pain, other Prospective Study
1. Zuyderland Medical Center, 2. Catharina Hospital, 3. Laurentius Hospital, 4. Maastricht University Medical Center
Presenter
Links

Abstract

Hypothesis / aims of study
Outpatient intravesical OnabotulinumtoxinA (BoNTA) is a well-established treatment for refractory overactive bladder (OAB) (1). However, there is a large variety in pain management during the procedure (e.q under general anethesia at the operation room, using sedatives or intravesical anesthetics). Previous studies suggest that lidocaine may have a limited effect on pain perception (2,3). This study evaluated whether lidocaine instillation provides analgesic benefit compared to no local analgesia prior to BoNTA procedure, hypothesizing there is no clinically relevant difference in pain perception.
Study design, materials and methods
This prospective observational study was conducted at four hospitals in the Netherlands. Patients underwent either BoNTA injections after an intravesical lidocaine instillation or with no intravesical analgesia, based on the standard local practice. In three hospitals patients received lidocaine instillation and in one hospital patients received no analgesia. Pain was assessed by Numeric Rating Scale (NRS) at five time points; before initiation of the procedure, after reaching the bladder with the cystoscope, after the first injection, after the fifth injection and after the tenth injection. The sample size with a significance level of 0.01 (compensated for repeated testing with Bonferroni method), a power of 80%, a ratio of 1:1, allowable difference of 0, standard deviation (SD) of 2, margin of 1 is used. With an expected dropout rate of 10%, a sample size is calculated at 116 participants per group, leading to a total sample size of 232 patients. Multivariable linear mixed models were performed to adjust for confounding factors. Secondary outcomes included patient satisfaction at the time of procedure, cost, and carbon footprint (kgCO₂e) associated with lidocaine use. Patient satisfaction was measured using an validated questionnaire.
Results
A total of 232 patients were included (lidocaine: n=116; no-analgesia: n=116). The baseline characteristic (age, sex, BMI, indication) of patients were similar in both groups. The mean NRS score over the five time-measurements was for the lidocaine group 2.2 (SD 1.6) and for the no-analgesia group 2.3 (SD 1.7), there was no significant difference between the two groups. Multivariable analyses showed no independent association between lidocaine instillation and pain scores over time (figure 1). All procedures were completed successfully. Patient satisfaction was high. A total of 98.6% of respondents who completed the questionnaire reported some degree of satisfaction, with no significant difference observed between the two groups. Omitting lidocaine saved €14.06 per procedure and reduced carbon emissions by 3.255 kgCO₂e.
Interpretation of results
Addition intravesical instillation with lidocaine prior to outpatient BoNTA injections did not result in clinical relevant lower NRS scores. These results are consistent with previous research suggesting limited analgesic benefit of lidocaine for this procedure. Additionally, patient satisfaction remained high in both groups, supporting the feasibility of omitting lidocaine.
Concluding message
Intravesical instillation with lidocaine does not appear to provide clinically significant analgesic benefit. Eliminating its routine use could enhance procedural efficiency, reduce healthcare costs, and lower environmental impact without compromising patient comfort and satisfaction
Figure 1
References
  1. Lin Y-H, Chiang B-J, Liao C-H. Mechanism of action of botulinum toxin A in treatment of functional urological disorders. Toxins. 2020;12(2):129
  2. Pereira e Silva R, Ponte C, Lopes F, Palma dos Reis J. Alkalinized lidocaine solution as a first-line local anesthesia protocol for intradetrusor injection of onabotulinum toxin A: Results from a double-blinded randomized controlled trial. Neurourology and Urodynamics. 2020;39(8):2471-9.
  3. Negrean C, Ross J, Yu W, Maciejewski C, Vigil HR, Hickling D. Lidocaine solution vs. lidocaine gel instillation for pain management during intravesical botulinum injections. Canadian Urological Association Journal. 2025;19(6):189.
Disclosures
Funding None Clinical Trial No Subjects Human Ethics Committee METC Zuyderland Helsinki Yes Informed Consent Yes AI Not at all
Citation

Continence 19S (2026) 102684
DOI: 10.1016/j.cont.2026.102684

01/11/2026 13:08:18