Non-Invasive Assessment of Wound Healing With Optical Methods

NCT00578604 | Completed

• 1 other identifier: 17035
• Study Type: observational
• Target: 38
• Locations: 1 country
• Sites: 1

Brief Summary

The objective of this project is to further the development of a non-invasive optically based NIR (Near Infrared) device to enable the quantitative diagnosis, monitoring and treatment optimization of chronic wounds (especially diabetic) in a clinical setting. The end goal of this project is a portable and compact device that would be simple to operate by minimally trained health care personnel. Our animal studies have shown that the early healing of chronic wounds can be characterized by absorption and scattering of light at near infrared wavelengths ranging from 680 nm to 950 nm. If our project is successful we will be providing the clinician the ability to predict if a wound is healing and if a particular treatment is successful in accelerating healing before any changes are observed by wound size contraction or other visible clinical signs. Our hope is that the fNIR optical device will provide conclusive therapeutic treatment information as early as 5 weeks after initial evaluation, before it would be obvious on gross examination of the patient.

Conditions

Diabetic Foot Ulcers

Outcome Measures

Primary Outcomes (1)

• diffuse near infrared spectroscopy measurements

  The end goal of this project is a portable and compact device that would be simple to operate by minimally trained health care personnel and is comparable to SOC doppler.

  3 years

Study Arms (2)

Patients with a diabetic wound

Patients with a diabetic wound

Device: diffuse near infrared spectroscopy measurements

Control

Patients without a diabetic wound

Device: diffuse near infrared spectroscopy measurements

Interventions

diffuse near infrared spectroscopy measurements DEVICE

Measure blood flow to diabetic wounds

Control; Patients with a diabetic wound

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Recruited patients will be patients with diabetes who have chronic wounds and will likely have other co-morbidities associated with chronic diabetes. Control subjects do not have diabetes and do not have wounds.

You may qualify if:

• Subjects must be 18-65 years of age
• Subjects must have no history of diabetes
• Subjects must have no history of vascular disease
• Subjects must have no findings of vascular disease on physical examination
• Subjects who are not allergic to Tegaderm
• Subjects must be 18-65 years of age
• Subjects must have documented diabetes mellitus for at least 6 months.
• Subjects must have at least one documented chronic wound for a minimum 8 weeks.
• A chronic wound is defined as any wound that has not healed after 8 weeks and has a minimum surface area of 1cm2. There is no maximum wound size.
• Wound(s) must be secondary to the complications of diabetes, including vascular disease neuropathy, or both.
• Wounds must be on the ankles or feet
• Subjects who are not allergic to Tegaderm

You may not qualify if:

• Subject must not be \<18 or \>65 years of age
• Subjects with major infections, abscesses, or untreated osteomyelitis will be excluded until appropriately treated.
• Subjects will not be excluded based upon the existence of other co-morbidities associated with chronic diabetes, including retinopathy, nephropathy, peripheral neuropathy, or cardiovascular disease except as follows:
• Subjects who have moderate to severe vascular insufficiency (defined as ankle brachial index \<0.75 or toe-brachial index \<0.5)
• Subjects who are unable to return for weekly follow-up appointments will not be included.
• Pregnant or lactating people will not be invited to participate.
• Subjects who are allergic to Tegaderm

Sponsors & Collaborators

• Drexel University College of Medicine: lead

Study Sites (1)

Drexel University College of Medicine Wound Care Center

Philadelphia, Pennsylvania, 19102, United States

Location

MeSH Terms

Conditions

Diabetic Foot

Condition Hierarchy (Ancestors)

Diabetic Angiopathies; Vascular Diseases; Cardiovascular Diseases; Foot Ulcer; Leg Ulcer; Skin Ulcer; Skin Diseases; Skin and Connective Tissue Diseases; Diabetes Complications; Diabetes Mellitus; Endocrine System Diseases; Diabetic Neuropathies

Study Officials

• Michael S Weingarten, M.D.

  Drexel University College of Medicine

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 20, 2007
• First Posted: December 21, 2007
• Study Start: September 1, 2007
• Primary Completion: June 1, 2014
• Study Completion: June 1, 2014
• Last Updated: March 30, 2017

Record last verified: 2017-03

Locations

US (1)