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Acute Effects of Whole Body Blue Light Exposure on Blood Pressure

Acute Effects of Whole Body Blue Light Exposure on Blood Pressure, Endothelial Function and Vascular Stiffness

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03226587
Enrollment
20
Registered
2017-07-24
Start date
2016-08-31
Completion date
2017-08-31
Last updated
2017-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blue Light

Keywords

blue light, blood pressure, vascular function, endothelial function, health volunteers

Brief summary

Ultraviolet light exposure was shown to be able to release nitric oxide from the skin into the blood stream and lead to an acute decrease in blood pressure and increase in vascular function. Additionally, preliminary work indicates that UV free blue light also releases nitric oxide in the skin mediating similar effects as seen with ultraviolet light A(UVA). It is the goal of the present experimental study to investigate the hemodynamic effects of whole body blue light exposure including blood pressure, endothelial function and vascular stiffness. Therefore, healthy volunteers will be exposed to 30 minutes whole body blue light (453 nm wavelength) and the change in blood pressure and endothelial function (Flow mediated dilation (FMD)), heart rate, forearm-blood flow, forearm vascular resistance central blood pressure and vascular stiffness ( pulse wave analysis by sphygmocor) will be measured. In this randomized controlled cross-over study, 20 healthy subjects aged 30 to 60 years will participate.

Interventions

PROCEDUREBlue light

Subjects will be exposed to blue light (453 nm wavelength) for 30 minutes

PROCEDUREcontrol exposure

Subjects will get control exposure to 30 minutes of whole body, which causes only comparable warming of skin as with blue light exposure.

Sponsors

Philips GmbH, Innovative Technologies, Aachen
CollaboratorUNKNOWN
Klinik für Unfall - und Handchirurgie, Universitätsklinikum Düsseldorf
CollaboratorUNKNOWN
Heinrich-Heine University, Duesseldorf
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
MALE
Age
30 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy, male subjects * age between 30 and 60 years * signed patient informed consent

Exclusion criteria

* diabetes mellitus * acute inflammation (CRP \>0.5mg/dl) * cardiac arrythmia * active cancer * renal failure * heart failure (NYHA II-IV) * arterial hypotension (systolic pressure \<100 mmHg) * treatment with antihypertensive drugs * dermatosis of the eyelid * porphyria or hypersensitivity to porphyrins * congenital or aсquired immune deficiency * genetic conditions that cause an increased sensitivity to light or an increased risk to dermatological cancer (such as xeroderma pigmentosum, cockayne syndrome, bloom syndrome) * previous intake or use of photosensitizing drugs, food or cosmetics (e.g. psychiatric medication, antibiotics, cardiovascular drugs, hormone, Hypericum, Bergamot orange) or use of perfumes

Design outcomes

Primary

MeasureTime frameDescription
Change of peripheral blood pressurebaseline, during 30 min exposure and 2 hours thereafterChange of peripheral blood pressure as measured before, during and up to 2 hours after 30 min blue light as compared to control

Secondary

MeasureTime frameDescription
Change in endothelial functionbaseline, during 30 min exposure and 2 hours thereaftermeasured by flow mediated dilation (FMD) before, immediately after 30 min exposure and at 2 h thereafter
Change from baseline heart ratebaseline, during 30 min exposure and 2 hours thereaftermeasured by electrocardiography (ECG) before, during and up to 2 hours after 30 min blue light as compared to control
Change from baseline forearm blood flowbaseline, during 30 min exposure and 2 hours thereaftermeasured by ultrasound before, immediately after 30 min exposure and at 2 h thereafter
Change from baseline central blood pressurebaseline, during 30 min exposure and 2 hours thereaftermeasured by applanation tonometry before, immediately after 30 min exposure and at 2 h thereafter
Change from baseline forearm vascular resistancebaseline, during 30 min exposure and 2 hours thereaftermeasured by ultrasound before, immediately after 30 min exposure and at 2 h thereafter
Change from baseline NO-speciesbaseline, during 30 min exposure and 2 hours thereafterdetermined by chemiluminescence before, immediately after 30 min exposure and at 2 h thereafter
Change from baseline Cortisolbaseline, during 30 min exposure and 2 hours thereaftermeasured before, immediately after 30 min exposure and at 2 h thereafter
Change from baseline Endorphinsbaseline, during 30 min exposure and 2 hours thereaftermeasured before, immediately after 30 min exposure and at 2 h thereafter
Change from baseline vascular stiffnessbaseline, during 30 min exposure and 2 hours thereaftermeasured by applanation tonometry before, immediately after 30 min exposure and at 2 h thereafter

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026