U.S., June 12 -- ClinicalTrials.gov registry received information related to the study (NCT07641218) titled 'Pilot Study of the ARTUS(R) Artificial Urinary Sphincter on Women' on June 01.
Brief Summary: The subjects will be implanted with the ARTUS(R) medical device and then be followed up to 2 years post-implantation, with the primary endpoints measured at 3-month post-implantation. Safety and Clinical performance outcomes will be measured for each subject at baseline (before implantation) and post-implantation.
Study Start Date: June 30
Study Type: INTERVENTIONAL
Condition:
Urinary Incontinence , Stress
Intervention:
DEVICE: Artificial Urinary Sphincter ARTUS
The subjects will be implanted by the ARTUS Artificial Urinary Sphincter...