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Organ Retractor Device Study

Recruiting
Conditions
Liver Retraction During Bariatric Surgery
Registration Number
NCT06754514
Lead Sponsor
Boehringer Labs LLC
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
150
Inclusion Criteria
  • undergoing minimally invasive primary bariatric surgery
Exclusion Criteria
  • known liver disease

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Ease of use and FeasibilityDuring surgery

After surgery, surgeons will be asked a series of questions and asked to rank the ease of use on a scale of 1-10

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

WakeMed Health & Hospitals

🇺🇸

Raleigh, North Carolina, United States

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