Use of Real-time Fluorescence Imaging in Diabetic Foot Ulcers: the Impact of Colonization
Infection, Surgical Site
About this trial
This is an interventional treatment trial for Infection, Surgical Site focused on measuring diabetic foot ulcer, non-infected, autofluorescence, fluorescence imaging, MolecuLight, artificial dermis, split thickness skin graft
Eligibility Criteria
Inclusion Criteria: 20 ≤ age < 80 Body mass index (BMI) < 35 kg/m2 Glycated hemoglobin (HbA1c) < 10% Target ulcer: (1) 10 ≤ size < 100 cm2 (2)Located on or below malleolus (3)Wagner's grade 2 or 3 initially (4)Margin > 3 cm between target ulcer and other ulcers Transcutaneous oxygen pressure (TcPO2) ≥ 30 mmHg and 0.8 ≤ ankle-brachial index (ABI) ≤ 1.2 Patient willingness and signed informed consent Exclusion Criteria: Pregnancy Type I diabetes mellitus (Type I DM) Active malignancy Taking glucocorticoids, immunosuppressants, or in an immunocompromised status Lab test upon admission for reconstruction surgery: (1) hemoglobin (Hb) < 8.0 g/dL, or white blood cell (WBC) < 3000 cell/μg (2) aspartate aminotransferase (AST) / alanine aminotransferase (ALT) / total bilirubin > 3x upper normal limits (3) albumin < 2.5 g/dL
Sites / Locations
- Shuang Ho Hospital First Medical Building
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Fluorescence-guided
Control
Patients who used MolecuLight to achieve "high-quality de-colonization" during reconstruction surgery with artificial dermis or split-thickness skin graft
Patients who did not use MolecuLight to achieve "high-quality de-colonization" during reconstruction surgery with artificial dermis or split-thickness skin graft