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...