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Thermal Screening for Early Diabetic Peripheral Neuropathy (DPN)

V

VisionQuest Biomedical

Status

Completed

Conditions

Diabetic Foot
Diabetic Neuropathies
Diabetic Retinopathy

Treatments

Other: no intervention

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT03069729
R43DK104578-01

Details and patient eligibility

About

The goal of this research is to develop better tools for diagnosing illness of the feet and legs of people who have diabetes. Investigators will use thermal videos of the foot to aid in the refinement of a system designed to detect signs of diabetic peripheral neuropathy (DPN). The team of investigators will also look at diabetic eye disease and how it might relate to diabetic foot disease.

Full description

This study focuses on further development and testing of a microvascular functional imaging system, a computer-based system for screening thermal video images, designed to detect biomarkers of diabetic peripheral neuropathy (DPN). Additionally, severity levels of diabetic retinopathy (DR) will be compared with those of DPN.

All participants in this study will undergo foot exams, thermal imaging of the foot, and standard retinal imaging. These non-invasive assessments will be performed at an initial study visit. Some of the participants will be offered additional study visits. One of the additional visits involves a standard nerve conduction velocity assessment by a neurologist, the other involves a DPN exam by a podiatrist.

Portions of the study take place at University of New Mexico Health Sciences Center (UNM HSC). The research utilizes services of the Clinical Translational Science Center (CTSC).

The study is approved by University of New Mexico Health Sciences Center's Human Research Review Committee (HRRC), which coordinates and supports the activities of the three federally mandated Human Research Review Committees (HRRCs) responsible for reviewing and approving all human research.

Enrollment

331 patients

Sex

All

Ages

35 to 76 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

• Must be non-diabetic or diagnosed as diabetic for at least 5 years

Exclusion criteria

history of chemotherapy

  • surgery below the knee within the last 2 years

  • fractures below the know within the last 2 years

  • history of stroke

  • body mass index (BMI) greater than 35

  • history of heart failure

  • peacemaker or implantable cardiovascular defibrillator

  • high blood pressure (over 180/100)

  • end-stage renal (kidney) disease or renal (kidney) transplant

  • peripheral edema greater than 2+ (swelling of the feet or hands)

  • diabetic foot ulcers

  • foot sores

  • Raynaud's phenomenon

  • tobacco use within the last month.

  • treatment with glucocorticoids, including:

    • beclomethasone
    • betamethasone
    • budesonide
    • cortisone
    • dexamethasone
    • hydrocortisone
    • methylprednisolone
    • prednisolone
    • prednisone
    • triamcinolone

Trial design

331 participants in 3 patient groups

Control group
Description:
non-diabetic; no intervention
Treatment:
Other: no intervention
Diabetics without DPN
Description:
diabetics without DPN; no intervention
Treatment:
Other: no intervention
Diabetics with DPN
Description:
diabetics with DPN; no intervention
Treatment:
Other: no intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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