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Recruiting NCT02370199

Peripheral Blood Flow Responses to Electromagnetic Energy

No phase Interventional Exposure to Man-made Visible Light

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: 670 nm light, octafluropropane.
Who it may be relevant to
Registry conditions: Exposure to Man-made Visible Light. Basic parameters: 18 years — 59 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study evaluates 670 nm energy in the form of red light to stimulate blood flow changes in healthy adults. All participants will receive red light to their leg. They will also receive a continuous infusion of Definity (octafluoropropane) ultrasound contrast.

Detailed description

670 nm energy in the form of red light dilates isolated blood vessels. This study seeks to measure vessel dilation in human subjects exposed to this energy at different irradiance intensities (25 milliwatts (mW)/cm2 and 75 mW/cm2). The intent of this protocol is to measure blood flow in the gastrocnemius muscle before and after exposure to 670 nm light energy. This protocol will be performed in healthy subjects, who do not meet exclusion criteria. The study consists of one visit. Blood flow measurement will be performed using contrast enhanced ultrasound, a method by which ultrasound contrast is continuously infused into the blood stream. Ultrasound records images in the area of interest and flow is related to the intensity of the contrast in each image. After baseline blood flow images are collected, the subject will receive red light energy to the gastrocnemius muscle with concurrent blood flow measurements with contrast ultrasound. The subject will be monitored post procedure and the study will then be completed.

Interventions

  • Device 670 nm light
    670 nm light emitting diode will be placed 1 cm above the gastrocnemius muscle. The diode will not be in direct contact with the skin. Subjects will be exposed to 75 mW/cm2.
  • Drug octafluropropane
    Octofluoropropane will be administered as a continuous infusion prior to the initiation of 670 nm light in order to measure skeletal muscle blood flow.

Primary outcome measures

  • Change in blood flow (using octafluoropropane infusion and ultrasound) [Time frame: 10 minutes]

Eligibility criteria

Inclusion criteria

  • Participants will be healthy subjects over the age of 18.
  • Men and women will be recruited for participation.
  • All ethnicities will be included in this study.

Exclusion criteria

Exclusionary criteria include:

  • age under 18 years and those over 60 years of age,
  • those who are unable to understand the consent process,
  • those who cannot read or speak English,
  • a history of cancer,
  • peripheral artery disease,
  • diabetes mellitus,
  • active pregnancy,
  • hypersensitivity to perflutren contrast agents,
  • pulmonary hypertension,
  • chronic kidney disease,
  • active tobacco or drug use,
  • blood pressure over 160/90, BMI>30,
  • sickle cell disease, or
  • history of intracardiac shunt.

Additional exclusion criteria include:

  • a history of coronary artery disease,
  • heart failure,
  • the presence of an implanted defibrillator or pacemaker,
  • a history of heart murmur or rhythm disorder (atrial fibrillation, atrial tachycardia, or ventricular tachycardia),
  • neurological diseases such as stroke, and
  • any uncontrolled medical conditions.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Basic science

Study locations

United States · 1 center
  • Medical College of Wisconsin — Milwaukee

Identifiers

NCT: NCT02370199 · 22652

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗