Endostapler Gastric Bypass Study

NCT04712526 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2023-10-04

No results posted yet for this study

Summary

The goal of this prospective, post-market study is to evaluate safety and efficacy of the AEON™ Endostapler when used in laparoscopic Roux-en-Y gastric bypass surgery.

Conditions

Interventions

DEVICE

AEON Endostapler

Surgery with AEON Endostapler

Sponsors & Collaborators

  • Lexington Medical Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-01-18
Primary Completion
2023-11-30
Completion
2023-12-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Diseases

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 NCT04712526 on ClinicalTrials.gov