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Bladder Overactivity and Post-Botulinum Toxin Telemonitoring
Sponsor: University Hospital, Grenoble
Summary
Prospective, randomized, controlled, single-center study to compare the feasibility of home monitoring for patients receiving intradetrusor botulinum toxin injections with that of the usual hospital-based follow-up.
Official title: Bladder Overactivity and Post-Botulinum Toxin Telemonitoring: a Randomized, Controlled, Superiority Trial
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
112
Start Date
2026-03-02
Completion Date
2031-03-02
Last Updated
2026-01-30
Healthy Volunteers
No
Conditions
Interventions
home care
6-week follow-up visit: At home (The service provider will bring the necessary equipment for the various measurements and the questionnaires, and will explain their use to the patient. The provider will return to collect the equipment and perform a post-void residual (PVR) measurement 72 hours later.)