Organ Retractor Device Study

Boehringer Ingelheim

Status: Enrolling

Conditions: Liver Retraction During Bariatric Surgery

Treatments: Device: liver retraction

Study type: Observational

Funder types: Industry

Identifiers

NCT06754514

Retractor-01

Details and patient eligibility

About

This study aims to assess the safety and efficacy of an organ retraction device. The study is low risk as it is only being used in patients already undergoing primary robotic bariatric surgery.

Enrollment: 150 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• undergoing minimally invasive primary bariatric surgery

Exclusion criteria

• known liver disease