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Experiences With Automated Surgical Drainage in Cardiac Surgery

NCT03860363 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 28

Last updated 2020-07-17

No results posted yet for this study

Summary

The purpose of this study is to evaluate the Thoraguard Surgical Drainage System in a real-world clinical environment. It is believed that this system will offer functional and clinical benefits over the current standard of care system for the removal of surgical fluids following cardiac surgery. Observations, experiences, and outcomes in a single hospital setting will be collected for the Thoraguard Surgical Drainage System.

Conditions

Interventions

DEVICE

Blood drainage post cardiac surgery

Blood drainage post cardiac surgery with Thoraguard Surgical Drainage System.

Sponsors & Collaborators

Principal Investigators

  • Jack Boyd, MD · Stanford University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-22
Primary Completion
2020-03-30
Completion
2020-05-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

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 NCT03860363 on ClinicalTrials.gov