Infrared Wraps Effect on Oxygenation of Diabetics Arm, Feet and Lower Leg

July 12, 2022 updated by: Yale University

A Pilot Study of the Impact of Passive, Garment-based Infrared Therapy on Oxygenation in the Feet and Lower Legs of Patients With Diabetes

This study seeks to prove that wraps manufactured with infrared textile are capable of augmenting peripheral circulation in the lower legs, arm and feet of participants with Diabetes Mellitus. Infrared is currently used in saunas and various textiles as general wellness products that purport to improve various health conditions and augment microcirculation. This study is intended to investigate specifically whether wraps capable of harnessing infrared energy can improve oxygenation in the feet, arms and lower legs of diabetics using noninvasive transcutaneous oximetry to do so.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Infrared energy is a type of electromagnetic energy that is invisible, and is further subdivided into three subsets based on wavelength. Far infrared (FIR or IR-C) is a subset of energy in the infrared spectrum that is thought to transfer energy in the form of heat, perceived by thermoreceptors in the skin as radiant heat. FIR is thought to be both absorbed by the human body but is also emitted in the 3-50 micron range, with a peak output at 9.4 micron. The range of far infrared varies depending on which source is referenced but is generally felt to start at 3 to 5 microns. The use of FIR has been studied in various circumstances and thought to improve various biological functions via FIR heat lamps, saunas, ray devices and FIR emitting ceramics and fabrics. There are no short-term or long-term safety issues that have arisen in any studies thus far. As noted in the 2006 statement of the ICNIRP (International Commission on Non-Ionizing Radiation Protection), "…the contribution made by the IR-C spectral region (3-1,000 micron) is normally of no practical concern from a health hazard standpoint." FIR has been shown to increase blood flow in forearms, and access flow and survival of arteriovenous fistula in hemodialysis patients. An unpublished study, by McClue, reported an apparent increase in pedal circulation of approximately 10% using transcutaneous oxygen monitoring in healthy subjects wearing socks infiltrated with FIR emitting textiles. The mechanism of improving circulation is not entirely elucidated, however recent work suggests a role of increasing endothelial nitric oxide synthase, nitric oxide production and modulating profiles of circulating miRNAs (mircoRNA, small noncoding RNAs of ∼22nt in length which are involved in the regulation of gene expression at the posttranscriptional level).

Type 2 Diabetes prevalence has increased significantly over the past decade, with estimates from 2015 of 26 million Americans diagnosed and predicted to increase to 32 million by 2020. Both Type 1 and Type 2 Diabetes is well known to increase the risk of nontraumatic lower extremity amputation by, amongst other factors, impairing circulation to the feet through both peripheral arterial disease and microvascular dysfunction.

Noninvasive transcutaneous oximetry measurements of the leg have been validated as a valuable tool in assessing lower extremity circulation in both normal subjects and diabetic individuals.

This trial seeks to prove that exposure to IR, through the use of newly developed socks (wraps here with same material) that contain thermoreactive particles woven into textile, which both emit IR and reflect the IR back from the body, can augment circulation in the feet, arms and lower legs of diabetic subjects. Noninvasive transcutaneous oximetry will be used as the assessment modality. If this study confirms this hypothesis, future studies may be planned to determine if the use of a IR-containing textile can prevent new ulcers from forming in high risk patients and perhaps even speed the healing of prevalent foot ulcers.

Subjects will be recruited from both primary care and specialty medical offices who carry a diagnosis of Diabetes Mellitus, will be between the ages of 18 to 80 and will act as their own controls. The goal will be to enroll a minimum of one hundred (100) patients who will be evaluated noninvasively with transcutaneous oxygen measurements using Radiometer TCM (PeriFlux 5000) supplied by Radiometer America, Inc. Upon screening and after signing informed consent, patients will have ankle brachial index (ABI) measurements performed on both legs to exclude those who have severe peripheral arterial disease (ABI index or 0.4 or lower). Upon arrival on study day, subjects will have both feet evaluated by a registered nurse (RN), to ensure there are no signs of infection, active foot ulcers, or other open wounds. If there is any such evidence, the patients will be excluded from the trial and sent for further evaluation and treatment according to standard of care by their primary care clinicians or podiatrists.

Subjects will be placed on an exam table reclined at a 120-degree angle with legs extended and supported by leg rest. The TCPO2 machine will have been turned on prior to patient arrival for calibration. If necessary, any hair on the subject's foot or leg will be removed in the area of fixation ring application by a disposable razor. The subject will then have up to 3 fixation rings attached, used for measuring TCPO2, placed on the lower leg and foot. The fixation rings will be further secured around the circumference with medical tape, approximately 1 inch by 0.5 inch per piece to further enhance the seal. In a double blind fashion, subjects will be randomized to have either placebo or IR wraps placed in a sequential way. The wrap will be placed over the foot, arm and lower leg covering the fixation rings. Three drops of contact solution will be placed inside each fixation ring, followed by attachment of the electrodes. There will then be a 30 minute rest/stabilization period allowing for the TCPO2 to stabilize (stabilization phase).

The wraps will then be gently applied to the arm, feet and leg, while being careful not to disturb the fixation rings. The placebo wraps are identical in all ways to the study wrap, with the exception that the placebo wraps do not contain the proprietary thermoreactive minerals woven into the fabric. The active phase will then commence and continue for 60 minutes, with TCPO2 measurements taking place continuously and recorded at least every 10 minutes. At the end of the 60-minute study period, the leads will be removed, followed by the wraps. The fixation rings are not removed, however. The TCPO2 machine should be recalibrated after the leads are returned to the holding chamber, prior to the second half of the trial using the other wraps (either IR or placebo, whichever was not used in first session). There will then be a 10-minute break period, subjects will be allowed to use the restroom and may place loose foot coverings over their feet for ambulation. Following the subjects return to the exam table, the same above protocol will be followed, with 30 minutes of rest/stabilization after the leads are placed back on for the baseline readings prior to wrap placement. Repeat TCPO2 measurements will be obtained according to the same schedule as indicated above. Activity will be restricted during the active and stabilization phase of the protocol. Patients will be encouraged to void prior to initiation of each half of the protocol. However, should subjects have to use the bathroom during one of the active phases, the rest and stabilization phase will restart at time zero following the bathroom break and reattachment of the TCPO2 sensors. At the completion of the study, the leads and fixation rings will be removed and subjects will return placebo and study socks to the appropriate personnel.

Study Type

Interventional

Enrollment (Actual)

39

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Connecticut
      • Hamden, Connecticut, United States, 06517
        • Endocrine Associates Of Connecticut

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patient with Type 1 or Type 2 Diabetes Mellitus between the ages of 18 and 80 years old.

Exclusion Criteria:

  • Chronic kidney disease treated by dialysis or those with a eGFR<30 mL/min/1.73m2
  • Alcohol or any illicit substance abuse
  • Use of systemic corticosteroids within previous 3 months
  • Has ever received immunosuppressive agents
  • Has ever undergone radiation therapy
  • Has ever used cytotoxic agents
  • Pregnant, breast-feeding or attempting to become pregnant
  • History of known peripheral arterial disease or lower extremity amputation
  • Any neurologic disease or other condition preventing normal ambulation
  • History of significant trauma to the lower extremities, major orthopedic or neurological damage to the lower extremities
  • History of saphenous venous graft harvesting
  • Ankle-Brachial Index of 0.40 or lower
  • Any ulcer or open wound on the lower extremities
  • Inability to lie flat for up to 90 minutes at a time
  • Any symptoms within past 21 days of cough, fever, sore throat, chills, body aches, shortness of breath, loss of smell, loss of taste, fever at or greater than 100 degrees Fahrenheit
  • COVID positive nasal swab within past 21 days

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: Placebo Sock
Placebo Socks will be placed on participants feet either first or second for 60 minutes
Device: Active IR sock
Subjects will be wearing the infrared socks for 60 minutes
Other Names:
  • Infrared sock
Other: Placebo socks
Placebo Socks will be placed on participants feet first for 60 minute
Active Comparator: Active IR Sock
Active IR socks will be placed on participants feet either first or second
Device: Active IR sock
Subjects will be wearing the infrared socks for 60 minutes
Other Names:
  • Infrared sock
Other: Placebo socks
Placebo Socks will be placed on participants feet first for 60 minute

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in oxygenation of feet and lower legs
Time Frame: 60 minutes
Transcutaneous oxygen measurements will be compared between placebo and active IR sock
60 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Yale University

Collaborators

CIRCUFIBER, Inc.

Investigators

  • Principal Investigator: Adam B Mayerson, M.D., Yale School of Medicine

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 26, 2021

Primary Completion (Actual)

July 12, 2022

Study Completion (Actual)

July 12, 2022

Study Registration Dates

First Submitted

July 1, 2020

First Submitted That Met QC Criteria

July 1, 2020

First Posted (Actual)

July 7, 2020

Study Record Updates

Last Update Posted (Actual)

July 14, 2022

Last Update Submitted That Met QC Criteria

July 12, 2022

Last Verified

July 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 2000027079

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

There is no current plan to share IPD.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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