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Use of Real-time Fluorescence Imaging in Diabetic Foot Ulcers: the Impact of Colonization

Primary Purpose

Infection, Surgical Site

Status
Active
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
MolecuLight
Sponsored by
Taipei Medical University Shuang Ho Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

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

20 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

No Intervention

Arm Label

Fluorescence-guided

Control

Arm Description

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

Outcomes

Primary Outcome Measures

Complete healing time
The time for complete wound epithelialization or closure without drainage after reconstruction surgery.
Wound healing rate on 30, 60, 90 and 180 days
The healing percentage of wound 30, 60, 90 and 180 days after reconstruction surgery.
Artificial dermis (AD) or split-thickness skin graft (STSG) take rate
The take percentage of artificial dermis or split-thickness skin graft 21 days after reconstruction surgery.

Secondary Outcome Measures

Percentage of bacteria before MolecuLight de-colonization
The percentage of bacteria after the last debridement without using MolecuLight to do de-colonization.
Percentage of bacteria after MolecuLight de-colonization
The percentage of bacteria after using MolecuLight to do de-colonization.
Wound surface area on 30, 60, 90 and 180 days
The surface area of wound 30, 60, 90 and 180 days after reconstruction surgery.
Reasons for poor AD or STSG take rate
Reasons for poor take rate of artificial dermis or split-thickness skin graft 21 days after reconstruction surgery may include as follows: (1) weak graft fixation (2) seroma (3) hematoma (4) wound localized infection (5) osteomyelitis (6) irreversible ischemic ulcers (7) systemic cause
Complications on 180 days
Complications evaluated 180 days after reconstruction surgery may include as follows: (1) wound recurrence (2) higher-level amputation (3) above or below knee amputation (4) vascular restenosis (5) mortality
Vancouver scar score on 180 days
The vancouver scar score of wound evaluated 180 days after reconstruction surgery.

Full Information

First Posted
June 14, 2022
Last Updated
May 15, 2023
Sponsor
Taipei Medical University Shuang Ho Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05873049
Brief Title
Use of Real-time Fluorescence Imaging in Diabetic Foot Ulcers: the Impact of Colonization
Official Title
Use of Real-time Fluorescence Imaging in Diabetic Foot Ulcers: A New Strategy to Assess Residual Bacterial Colonization Before Application of Artificial Dermis or Split-thickness Skin Graft
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 1, 2022 (Actual)
Primary Completion Date
March 31, 2024 (Anticipated)
Study Completion Date
October 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Taipei Medical University Shuang Ho Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
The study evaluates the efficacy of fluorescence-guided de-colonization in patients with non-infected diabetic foot ulcers. The efficacy will also be compared between those who used artificial dermis and split-thickness skin graft for reconstruction surgery.
Detailed Description
Diabetic foot ulcers (DFU) are the main cause of hospitalization in diabetic patients. These hard-to-heal ulcers have a high amputation rate, and a 5-year mortality rate of 50% once being amputated. Treatments for DFU include infection management, wound debridement, revascularization, pressure off-loading, etc. Recently, a novel imaging device called MolecuLight i:X was introduced to help visualize clinically undetectable fluorescent bacteria in wounds and has shown promising effects in the identification of infection. However, as microorganisms almost colonize all chronic wounds, the term "bacterial colonization" should be distinguished from clinical infection. While infection delays the healing process, the impact of colonization on wound reconstruction remains unclear; and the assessment is often more difficult on DFU patients with peripheral neuropathy and vascular diseases. In the present study, investigators will conduct a prospective randomized controlled trial to evaluate the clinical outcome of achieving "high-quality de-colonization" with the aid of MolecuLight i:X in the treatment of noninfected DFU patients, and to compare its efficacy between artificial dermis and split-thickness skin graft.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infection, Surgical Site
Keywords
diabetic foot ulcer, non-infected, autofluorescence, fluorescence imaging, MolecuLight, artificial dermis, split thickness skin graft

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
210 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Fluorescence-guided
Arm Type
Experimental
Arm Description
Patients who used MolecuLight to achieve "high-quality de-colonization" during reconstruction surgery with artificial dermis or split-thickness skin graft
Arm Title
Control
Arm Type
No Intervention
Arm Description
Patients who did not use MolecuLight to achieve "high-quality de-colonization" during reconstruction surgery with artificial dermis or split-thickness skin graft
Intervention Type
Device
Intervention Name(s)
MolecuLight
Intervention Description
MolecuLight is a handheld fluorescence imaging device that is utilized to help real-time visualize clinically undetectable fluorescent bacteria in wounds. It emits a 405 nm wavelength of safe violet light, which interacts with the wound tissue and bacteria causing certain bacteria to emit red or cyan fluorescence. The fluorescence signals were then captured by MolecuLight and those with bacteria at levels of ≥ 10^4 colony forming units per gram (CFU/g) will be detected and displayed on the screen.
Primary Outcome Measure Information:
Title
Complete healing time
Description
The time for complete wound epithelialization or closure without drainage after reconstruction surgery.
Time Frame
180 days after reconstruction surgery
Title
Wound healing rate on 30, 60, 90 and 180 days
Description
The healing percentage of wound 30, 60, 90 and 180 days after reconstruction surgery.
Time Frame
180 days after reconstruction surgery
Title
Artificial dermis (AD) or split-thickness skin graft (STSG) take rate
Description
The take percentage of artificial dermis or split-thickness skin graft 21 days after reconstruction surgery.
Time Frame
21 days after reconstruction surgery
Secondary Outcome Measure Information:
Title
Percentage of bacteria before MolecuLight de-colonization
Description
The percentage of bacteria after the last debridement without using MolecuLight to do de-colonization.
Time Frame
Immediately after last debridement
Title
Percentage of bacteria after MolecuLight de-colonization
Description
The percentage of bacteria after using MolecuLight to do de-colonization.
Time Frame
Immediately after de-colonization with MolecuLight
Title
Wound surface area on 30, 60, 90 and 180 days
Description
The surface area of wound 30, 60, 90 and 180 days after reconstruction surgery.
Time Frame
30, 60, 90 and 180 days after reconstruction surgery
Title
Reasons for poor AD or STSG take rate
Description
Reasons for poor take rate of artificial dermis or split-thickness skin graft 21 days after reconstruction surgery may include as follows: (1) weak graft fixation (2) seroma (3) hematoma (4) wound localized infection (5) osteomyelitis (6) irreversible ischemic ulcers (7) systemic cause
Time Frame
21 days after reconstruction surgery
Title
Complications on 180 days
Description
Complications evaluated 180 days after reconstruction surgery may include as follows: (1) wound recurrence (2) higher-level amputation (3) above or below knee amputation (4) vascular restenosis (5) mortality
Time Frame
180 days after reconstruction surgery
Title
Vancouver scar score on 180 days
Description
The vancouver scar score of wound evaluated 180 days after reconstruction surgery.
Time Frame
180 days after reconstruction surgery.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shun-Cheng Chang, Director
Organizational Affiliation
Taipei Medical University Shuang Ho Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shuang Ho Hospital First Medical Building
City
New Taipei City
ZIP/Postal Code
235
Country
Taiwan

12. IPD Sharing Statement

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Use of Real-time Fluorescence Imaging in Diabetic Foot Ulcers: the Impact of Colonization

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