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Registry for Quality Assessment With Ultrasound Imaging and TTFM in Cardiac Bypass Surgery

NCT02385344 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1046

Last updated 2018-09-07

No results posted yet for this study

Summary

The purpose of the registry is to collect information regarding the number and type of coronary artery bypass (CAB) surgical procedure changes that are made based on intraoperative guidance information using transit time flow measurements (TTFM) and ultrasound image capabilities provided with the Medistim device.

Conditions

  • Coronary Artery Bypass

Interventions

DEVICE

Medistim device

This registry is intended to document surgical findings, procedural changes, and adverse events occurring prior to discharge

Sponsors & Collaborators

  • Medistim ASA

    lead INDUSTRY

Principal Investigators

  • Anne Waaler, MSc Pharm · Medistim ASA

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2017-12-31
Completion
2017-12-31

Countries

  • United States
  • Canada
  • Germany
  • Italy
  • Netherlands
  • 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 NCT02385344 on ClinicalTrials.gov