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Experiences With New Digital Surgical Drainage System in Thoracic Surgery

NCT04068545 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

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 and air following thoracic surgery. Observations, experiences, and outcomes in a single hospital setting will be collected for the Thoraguard Surgical Drainage System.

Conditions

  • Pulmonary Air Leak

Interventions

DEVICE

Device: Thoraguard Surgical Drainage System

Fluid drainage following thoracic surgery

Sponsors & Collaborators

Principal Investigators

  • Michael Zervos, MD · NYU Langone Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-02
Primary Completion
2020-03-30
Completion
2020-05-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

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 NCT04068545 on ClinicalTrials.gov