MedTrace Logo

Wound Perfusion in High Risk Surgical Incisions

NCT04233307 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2020-01-21

No results posted yet for this study

Summary

This is a prospective cohort pilot study. The primary purpose is to report the perfusion status of the surgical field in at risk surgical incisions. The secondary purposes are to describe the relationship between perfusion status and wound healing status and complications, and to describe the relationship between infrared digital thermography perfusion readings and the timing of propofol infusion. The research intervention will be photographs taken of the wound on the injured extremity, with a Forward-Looking Infrared (FLIR) camera, for the purpose of assessing perfusion status and skin temperature at the surgical site.

Conditions

  • Bone Fractures Multiple

Interventions

DIAGNOSTIC_TEST

Telethermographic images

Infrared digital thermography photographs of fracture wound and contralateral limb before and after propofol infusion.

Sponsors & Collaborators

  • Florida Orthopaedic Institute

    lead NETWORK

Principal Investigators

  • Hassan Mir, MD · Florida Orthopaedic Institute

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-02-29
Primary Completion
2020-12-31
Completion
2021-12-31

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 NCT04233307 on ClinicalTrials.gov