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Retrospective Database Review at LTC and SNFs

NCT06068972 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 193

Last updated 2023-10-05

No results posted yet for this study

Summary

The goal of this observational study is to compare the differences in wound outcomes when the MolecuLight imaging procedure is used in combination with standard of care wound assessment in long term care and skilled nursing facilities. The main outcome studied is healing of ulcers after 12-weeks, along with other outcomes such as occurrence of infection, complications, and antimicrobial use. Medical records from the past were reviewed, where patients receiving the MolecuLight procedure were compared to those who did not.

Conditions

  • Non-Healing Ulcer of Skin
  • Autofluorescence Imaging

Interventions

DEVICE

MolecuLight

Point-of-care fluorescence imaging of high bacterial loads

Sponsors & Collaborators

  • Wound Care Plus, LLC

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-20
Primary Completion
2022-07-12
Completion
2023-06-19
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 NCT06068972 on ClinicalTrials.gov