Condition: Stress Urinary Incontinence · Pelvic Organ Prolapse · Sponsor: Ethicon, Inc.
The objective of this post market, clinical registry is to evaluate the performance of the products of the TVT family of products or vaginal vault or uterine prolapse repair (with laparotomic or laparoscopic approach including robotic assisted) using either Gynemesh PS Mesh or Artisyn Mesh in women undergoing surgery for SUI and POP.
This description comes directly from the study's public registry record.
Christine Romanowski · 908-808-6219 · cromanow@its.jnj.com
Always discuss trial participation with your own doctor first.
| Yale University | New Haven, Connecticut, United States | Recruiting |
| Duke University | Durham, North Carolina, United States | Recruiting |
| University of Pennsylvania | Philadelphia, Pennsylvania, United States | Recruiting |
| UPMC | Pittsburgh, Pennsylvania, United States | Recruiting |
| Krankenhaus der barmherzigen Schwestern | Linz, Austria | Recruiting |
| Herlev Hospital | Hillerød, Denmark | Not Yet Recruiting |
| Hopital Jeanne de Flandres | Lille, France | Not Yet Recruiting |
| Universitatsklinikum Tubingen | Tübingen, Germany | Active Not Recruiting |
| Bio-Medical University Rome | Rome, Italy | Recruiting |
| Karolinska Institute | Stockholm, Sweden | Recruiting |
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Source record: clinicaltrials.gov/study/NCT04829175