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Post Market Study for FloShield 10mm Reusable Cannula and Blunt Obturator and Robotic FloShield

NCT02163239 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2015-09-28

No results posted yet for this study

Summary

This study evaluates the use of the FloShield System with the FloShield 10mm reusable Cannula and Oburator during standard robotic laparoscopic single-site surgery. The study will evaluate the compatibility of the FloShield 10mm Cannula and Oburator with the daVinci® Robotic Surgical System during single-site laparoscopic surgery.

Conditions

  • Cholecystectomy
  • Benign Hysterectomy
  • Salingo-oophorectomy

Interventions

DEVICE

Cannula and Blunt Obturator

The FloShield 10mm Endoscopic Cannula and Blunt Obturator will be used to maintain access to the peritoneal cavity during robot-assisted single site laparoscopic surgery

Sponsors & Collaborators

  • Minimally Invasive Devices, Inc.

    lead INDUSTRY

Principal Investigators

  • Wayne Poll, MD · Minimally Invasive Devices

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2015-09-30
Completion
2015-09-30

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 NCT02163239 on ClinicalTrials.gov