Active Clearance Technology (ACT) Registry

NCT02682849 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2020-10-29

No results posted yet for this study

Summary

The purpose of this study is to evaluate the effectiveness of the PleuraFlow® Active Clearance Technology™ (ACT) System in the management of blood evacuation after cardiac surgery.

Conditions

  • Retained Blood Syndrome

Sponsors & Collaborators

  • John M. Stulak

    lead OTHER

Principal Investigators

  • John Stulak, M.D. · Mayo Clinic

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-10
Primary Completion
2018-05-31
Completion
2020-03-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT02682849 on ClinicalTrials.gov