Clin2
NCT07205445Possibly a fitRecruiting

Registry study of Tensi+ for overactive bladder

Overactive Bladder

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

This registry will track people with overactive bladder (either from an unknown cause or a nerve condition) who use the Tensi+ device. The device delivers mild electrical pulses to help control bladder symptoms.

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

Phase
N/A
Enrollment
500 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are 18 or older.
  • You have overactive bladder from an unknown cause or related to a nerve problem.
  • You do not have a pacemaker, defibrillator, or any other implanted electronic device.
  • You do not have metal implants near your ankle area.
  • You are not pregnant.
  • You have no ankle problems, swollen ankles, skin damage, or skin disease on the area where electrodes go.
  • You have no cognitive impairment that would prevent you from following instructions.

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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