Clinical Trials

Overview

About this study

The prupos of this study is to determine the long-term outcomes and symptoms resolution in patients who undergo robotic versus laparoscopic medial arcuate ligament release. Also, to study the intraoperative outcomes (operative time, blood loss, and conversion to open approach) and postoperative outcomes (including length of hospital stay and postoperative complications) of patients who undergo laparoscopic versus robotic median arcuate ligament release. We aim to determine if the median arcuate ligament release using a robotic approach provides optimal outcomes comparable to the laparoscopic median arcuate ligament release.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Participating Mayo Clinic locations

More information