InterStim Basic Evaluation Lead Post-Market Clinical Follow-up Study

  • STATUS
    Not Recruiting
  • participants needed
    100
  • sponsor
    MedtronicNeuro
Updated on 16 June 2021
neuromodulation

Summary

Post-market clinical follow-up for continued assessment of safety and performance of the InterStim basic evaluation lead and foramen needle(s) used during a therapy evaluation.

Details
Condition Urinary Incontinence, bladder disorder, Overactive Bladder, Urge Incontinence, Bladder Disorders, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome, Urgency-frequency Syndrome
Treatment InterStim Basic Evaluation lead and foramen needle
Clinical Study IdentifierNCT04016324
SponsorMedtronicNeuro
Last Modified on16 June 2021

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