NeuroGyn Genital Neuromodulation System
DeviceGenital Neuromodulation
NCT Number: NCT06529198
The NeuroGyn study is designed to evaluate the safety and effectiveness to the NeuroGyn Genital Neuromodulation System as an aid in the treatment of the symptoms of idiopathic overactive bladder in patients who have failed or could not tolerate more conservative treatments.
Trial opening soon.
Get Notified18 year–85 year
All sexes
Interventional
Not applicable
not provided
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Genital Neuromodulation
Time frame: 6 months - 1 year - 2 years follow up
Overactive Bladder Symptom Score - OABSS
Time frame: 6 months - 1 year - 2 years
Noninvasive uroflowmetry, followed by invasive cystometry and a pressure-flow study + concurrent electromyography (EMG) of pelvic floor muscles and urethral pressure profiles
Time frame: 6 months - 1 year - 2 years
International Consultation on Incontinence Questionnaire (ICIQ)
Time frame: 6 months - 1 year - 2 years
PHQ-9
Contact information is provided by the study sponsor or research team.
Prof. Dr. med. Marc Possover
Other
The NEUROGYN-GNS Pivotal Clinical Study to Assess the Safety and Efficacy of the Neurogyn Genital Neuromodulation System, a Genital Nerves Neuromodulation Device Used to Treat Idiopathic Overactive Bladder (iOAB).
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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