Robotic Minimally Invasive Inguinal Hernia Repair Post-Market Clinical Study With the DEXTER Robotic System
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
The purpose of this post-market, observational study is to collect data under anticipated conditions of use that demonstrates that DEXTER performs as intended in the intended patient population, including a variety of representative disease etiologies and demographic groups.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 22
Healthy Volunteers: f
View:
• Subject is ≥ 22 years of age at time of enrollment/consent
• Subject is indicated for and planned to undergo robot-assisted and laparoscopic surgery for unilateral or bilateral inguinal hernia repair
• Subject is able and willing to comply with the protocol requirements, has been informed of the nature of the study, and has signed the IRB-approved informed consent form
Locations
United States
New York
Northtowns Ambulatory Surgical Center (NASC)
NOT_YET_RECRUITING
Buffalo
Texas
Memorial Hermann-Texas Medical Center - UT Health Houston
RECRUITING
Houston
Contact Information
Primary
Pascal Lehmann
pascal.lehmann@distalmotion.com
+41215105890
Time Frame
Start Date: 2025-11-26
Estimated Completion Date: 2029-12
Participants
Target number of participants: 140
Related Therapeutic Areas
Sponsors
Leads: Distalmotion SA
Collaborators: Veranex, Inc.