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Diabetic Foot Ulcers Microbiome and Pathogen Identification

The Role of The Microbiome in Diabetic Foot Ulcers (DFU)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05556954
Enrollment
103
Registered
2022-09-27
Start date
2022-10-13
Completion date
2025-06-04
Last updated
2025-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Foot Ulcer, Diabetes Mellitus, Wound

Keywords

Wound Infection, Wound assessments, Wound's microbiome

Brief summary

This research is being done because people with diabetes have reduced healing capacity and prone to develop infections of foot wounds. This can be problematic because wounds that become infected may result in amputation and more severe complications. New evidence suggests that a better understanding of the microbiome of wounds (e.g., bacterial presence) may provide information about wound healing and provide an earlier opportunity to identify an individual who may be prone to develop diabetic foot infection in their wound. Therefore, the purpose of this study is to evaluate the role of the microbiome of the diabetic foot ulcer in development of infection and wound healing. Once the role of the microbiome is confirmed, progress towards the prevention and treatment of diabetic foot ulcers and complications may be possible.

Interventions

Participant that are having usual care visits for management of diabetic foot ulcers will be enrolled into this study. The procedure is done as part of standard of care. Tissue from the samples will be analyzed for this study. Aliquoting and Deoxyribonucleic acid (DNA) extraction will be done on the specimens. Bacterial DNA from biospecimens will be isolated, quantified, amplified, and sequenced.

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
University of Michigan
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* DFU patients with diabetes mellitus * Have a hemoglobin A1c\[HbA1c\] of 12% or less as measured within the last 6 months * Stated willingness to comply with all study procedures and availability for the duration of the study

Exclusion criteria

* Pregnant or lactating * Uncontrolled blood glucose as demonstrated by by a HbA1c of greater than 12% * Bilateral wound or ulcer * Current infection of Coronavirus (COVID-19) * Unable to provide informed consent or are unwilling to participate.

Design outcomes

Primary

MeasureTime frame
The percent change in foot ulcer surface area (cm2) after 12 weeks of observation for either infected or non-infected diabetic foot ulcersBaseline to 12 weeks

Secondary

MeasureTime frameDescription
Total days of antibiotic therapy for the DFU infected diabetic foot ulcer participantsBaseline to 12 weeks
Number of days to infection resolution for the DFU infected diabetic foot ulcer participantsBaseline to 12 weeks
The percent of clinically resolved infected DFU for infected diabetic foot ulcer participantsBaseline to 12 weeksDefined as improvement of greater or equal to 2 clinical signs (Local swelling or induration, erythema, local tenderness or pain, local warmth, purulent discharge) with no requirement for additional antibiotic(s).
Post-study percentage change of wound surface area (cm2) for both cohortsBaseline to 12 weeks
Proportion of participants that reach a 50% reduction in surface area of the DFU for both cohortsBaseline to 4 weeks
The percentage of participants with an infected DFU at baseline that resolve clinical infection by study week 4Baseline to 4 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026