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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 670 nm light | Experimental | Subjects will have baseline blood flow measured in the gastrocnemius using octafluoropropane infusion and ultrasound.After baseline flow measurements are obtained, a 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. Contrast images will be obtained up to 5 minutes after the commencement of light. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 670 nm light | Device | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in blood flow (using octafluoropropane infusion and ultrasound) | Blood flow changes based on ultrasound imaging | 10 minutes |
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Inclusion Criteria:
Exclusion Criteria:
Exclusionary criteria include:
Additional exclusion criteria include:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Nicole L Lohr, MD, PhD | Contact | 205-996-3504 | nlohr@uabmc.edu |
| Name | Affiliation | Role |
|---|---|---|
| Nicole L Lohr, MD, PhD | Medical College of Wisconsin | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Medical College of Wisconsin | Recruiting | Milwaukee | Wisconsin | 53226 | United States |
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| ID | Term |
|---|---|
| D014467 | Ultraviolet Therapy |
| C042852 | perflutren |
| ID | Term |
|---|---|
| D010789 | Phototherapy |
| D013812 | Therapeutics |
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| octafluropropane | Drug | Octofluoropropane will be administered as a continuous infusion prior to the initiation of 670 nm light in order to measure skeletal muscle blood flow. |
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