Clin2
NCT07379372Possibly a fitNot yet recruiting

Telemonitoring after bladder botulinum toxin injections

Overactive Bladder

Part of Kidney & urinary, Women’s health & pregnancy clinical trials.

This study is testing a new way to monitor patients after they receive botulinum toxin injections for an overactive bladder. Instead of going to the clinic, a care provider will visit you at home to help track your symptoms and recovery.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
112 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You have a bladder condition caused by nerve damage (neurogenic bladder) or an overactive bladder without a known cause.
  • You are already receiving or will receive botulinum toxin injections into the bladder as part of your regular care.
  • You can have a home visit from a service provider in the area covered by the AGIR à dom group.
  • You are enrolled in the French social security system.
  • You agree to take part and provide informed consent.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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