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A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technology

NCT02500537 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2017-04-04

Study results available
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Summary

A post-market study of the Endo GIA™ Reinforced Reload with Tri-Staple™ Technology.

Conditions

  • Non-emergent, Abdominal or Thoracic Procedures

Interventions

DEVICE

Endo GIA™ Reinforced Reload with Tri-Staple™ Technology

Endo GIA™ Reinforced Reload with Tri-Staple™ Technology (Universal Handle)

Sponsors & Collaborators

  • Medtronic - MITG

    lead INDUSTRY

Principal Investigators

  • Ahmed Ahmed, PhD, FRCS · St Mary's Hospital, London

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2016-05-31
Completion
2016-08-31

Countries

  • United Kingdom

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 NCT02500537 on ClinicalTrials.gov