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Completed

NCT Number: NCT02798640

Comparative Study Evaluating Performance of Celliant Fibers on Tissue Oxygenation

The study will evaluate changes in transcutaneous oxygen tension (tcPO2,), and the inferred change in local cutaneous blood flow, in healthy subjects wearing a control and a 100% Celliant® fiber upper torso garment.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hologenix, LLC

Santa Monica, California, 90403, United States

About this study

Adequate blood supply is necessary for many physiologic processes. However, there are few valid, reproducible, non-invasive methods with which to assess it. One such measure is transcutaneous partial pressure of oxygen (tcPO2). This measurement is a non-invasive method of measuring oxygen tension at the skin surface; represents the amount of oxygen diffusing outward across the skin; and can be used as a surrogate for arterial perfusion. This method is reproducible with clinically acceptable intrasubject variability; is used for a variety of conditions, including peripheral vascular disease evaluation, predicting the outcome of patients requiring amputation and survival of skin grafts; and correlates well to angiography and increases in blood flow rates. However, tcPO2 is affected by many variables, including oxygen concentration in inspired air, lung function and hemoglobin saturation, as well as local factors, such as skin thickness, sympathetic tone, the presence of inflammation, capillary formation and skin oxygen consumption.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects greater than or equal to18 years of age
  • Men and women between the ages of 18 and 60 years
  • Able to understand and consent to the study
  • Able to follow directions of the Study Coordinators and/or the Principal Investigator
  • Able to complete the study
  • Male or female subjects of any ethnic origin such that the balance across ages and among population groups is reflective of the site population

Exclusion criteria

  • Active smokers
  • No history of cardiovascular disease
  • No history of peripheral vascular disease
  • Engaged in recreational drug use for the six months prior to the start of the study
  • Eaten within two (2) hours of the study
  • Consumed caffeine within four (4) hours prior to the study
  • Consumed alcohol with forty-eight (48) hours prior to the study
  • Subjects with any unstable medical or psychiatric problem
  • Subjects who are pregnant or nursing mothers
  • Subjects who are currently taking part in another clinical study or have taken part in a drug or device study, in the past month.

Treatment and study plan

Celliant

Device

100% Celliant garment

Control

Device

Control Garment

Primary outcomes

  1. Changes in transcutaneous oxygen tension (tcPO2)

    Time frame: 0,30,60,90 minutes

    comparison of individual measurements taken at these time points

Secondary outcomes

  1. Changes in local skin temperature by infrared imaging

    Time frame: 0,30,60,90 minutes

    comparison of individual measurements taken at these time points

Sponsors and collaborators

Lead sponsor

Kristopher Washington

Industry

Registry information

Official study title

A Single Center Prospective Comparative Study to Evaluate the Performance of a Upper Torso Garment Containing 100% Celliant Fibers That Emits Far Infrared (FIR) From Ceramic Particles Contained Within the Fibers in Healthy Subjects

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Jun 14, 2016
Registry last updated
Jun 14, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.