Organ Retractor Device Study

NCT06754514 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2025-01-01

No results posted yet for this study

Summary

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.

Conditions

  • Liver Retraction During Bariatric Surgery

Interventions

DEVICE

liver retraction

A different way to lift the liver during bariatric surgery

Sponsors & Collaborators

  • Boehringer Labs LLC

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-03-14
Primary Completion
2024-12-31
Completion
2025-01-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06754514 on ClinicalTrials.gov