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Evaluation of Tissue Oxygen Levels During Breast Reconstruction With a New Surgical Device

NCT03715270 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 6

Last updated 2019-06-10

No results posted yet for this study

Summary

This study is designed to evaluate the information provided to the clinicians by the surgical imaging device. It is also to gain insight on the user interface and how "user friendly" it is to the clinician.

Conditions

  • Perfusion; Complications

Interventions

DEVICE

Image surgical area

Image surgical area

Sponsors & Collaborators

  • Christie Medical Holdings, Inc.

    lead INDUSTRY

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-01-30
Primary Completion
2019-06-05
Completion
2019-06-05
FDA Device
Yes

Countries

  • United States

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 NCT03715270 on ClinicalTrials.gov