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MicroCutter in Surgical Stapling - European Trial I

NCT01476761 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 160

Last updated 2013-08-09

No results posted yet for this study

Summary

The purpose of this study is to evaluate safety of the Microcutter stapling /cutting device in patients requiring the transection, resection or anastomosis of gastrointestinal tissue in a post-market approval study.

Conditions

  • Thoracic

Interventions

DEVICE

Microcutter XPRESS and Microcutter XCHANGE

Surgical stapling devices

Sponsors & Collaborators

  • Cardica, Inc

    lead INDUSTRY

Principal Investigators

  • Andreas Kithe, M.D. · DRK-Krankenhaus Clementinenhaud, Hannover

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-11-30
Primary Completion
2013-06-30
Completion
2013-07-31

Countries

  • Germany

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 NCT01476761 on ClinicalTrials.gov