Actively Recruiting
Light Therapy in Patients Undergoing Surgery for Septic Joint, Necrotizing Soft Tissue Infection, Intraabdominal Sepsis, or Medical Treatment for Pneumonia
Led by Washington University School of Medicine · Updated on 2026-02-11
144
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
Sponsors
W
Washington University School of Medicine
Lead Sponsor
N
National Institute of General Medical Sciences (NIGMS)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying how exposure to bright blue light compared to standard white hospital lighting affects the immune response and organ function in adults undergoing treatment for pneumonia, septic joint surgery, necrotizing soft tissue infection surgery, or intraabdominal infection surgery. The study explores how light influences circadian clock proteins that regulate immune function, aiming to improve outcomes in serious infections and critical illness. This research builds on previous work showing blue light's impact on immune competence and tissue injury reduction. Participants will be randomly assigned to one of two groups: one group will be exposed to bright blue light (around 1700 lux, 442 nm spectrum) for 12 hours a day from 8:00 AM to 8:00 PM for three days, while the other group will receive standard ambient white fluorescent hospital lighting (300-400 lux) following the same schedule. The blue light is delivered using a small, portable device that participants will shine on themselves during the day for 72 hours. Both groups follow a 12-hour light and 12-hour dark cycle, with blue light turned off and filtered at night. During the study, participants will receive their standard medical or surgical care. Researchers will collect blood samples over the three days to measure inflammatory markers and circadian protein levels. Additional data such as white blood cell counts, heart rate, and infection complications will be monitored through medical records. The main outcomes include changes in inflammatory responses and organ dysfunction measured at the start and after 72 hours. The study aims to assess how blue light exposure may influence immune response and recovery in these infection-related conditions.
CONDITIONS
Brief Title
The Role of Circadian Clock Proteins in Innate and Adaptive Immunity
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 65 years
- Diagnosis requiring inpatient hospital care for one of the following: operation for intraabdominal infection, operation for necrotizing soft tissue infection, operation for infected joint, or medical treatment of pneumonia
You will not qualify if you...
- Traumatic brain injury
- Blindness
- Immunocompromised or immunosuppressed state
- Infection requiring treatment in the past 30 days
- Positive test for SARS-CoV-2 (COVID-19)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) during hospital stay at diagnosis
Duration - 3 days
Participants receive either blue light therapy or ambient white light as part of standard care after diagnosis or operation, for 3 days with a 12 hours:12 hours light:dark cycle.
Continuous light exposure daily from 8:00 AM to 8:00 PM for 3 days
Duration - 3 days concurrent with treatment
Participants have blood samples collected for research purposes to measure immune response and inflammatory mediators during the 3 days of light exposure. Clinical laboratory data are also abstracted from the electronic health record.
Six small blood sample collections over 3 days
Trial Site Locations
Total: 1 location
1
Barnes Jewish Hospital
St Louis, Missouri, United States, 63108
Actively Recruiting
Research Team
M
Matthew R Rosengart, MD MPH
X
Xianghong Zhang, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
8
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