drugset / Trial / NCT04270526

Minimizing Pain During Office Intradetrussor Botox Injection

NCT04270526

Phase 4 Completed 85 enrolled Boston Urogynecology Associates
RandomizedParallel-groupTriple-blindTreatment

Summary

This will be a prospective double-blinded randomized controlled trial comparing two pre-treatment protocols for patients undergoing intradetrussor botox injections to determine if a buffered lidocaine solution offers superior pain control.

Timeline

Start
2020-08-15
Primary completion
2023-06-30
Completion
2023-06-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator sodium bicarbonate Diagnostic / imaging agent 5 ml Other
Comparator sodium bicarbonate Diagnostic / imaging agent 8.4 % Other
Comparator Lidocaine Other / unclassified 1 % Other
Comparator Lidocaine Other / unclassified 50 ml Other