University of Illinois at Chicago
Chicago, Illinois, 60612, United States
Location status: Recruiting
Location contact
Sirimon Reutrakul, MD
CONTACT
NCT Number: NCT04547439
This study explores the use of melatonin in patients with diabetic retinopathy
Interested in participating?
Request Info40 year–65 year
All sexes
Interventional
Phase 2
Chicago, Illinois, 60612, United States
Location status: Recruiting
Sirimon Reutrakul, MD
CONTACT
This is a randomized controlled study using melatonin for 8 weeks in patients with diabetic retinopathy on outcomes of sleep and circadian regulation
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Melatonin 3 mg will be taken nightly for 8 weeks
Placebo will be given nightly for 8 weeks
Time frame: 14 days
Sleep pattern: Sleep duration and sleep efficiency will be assessed by wrist actigraphy, to be worn by the participants for 14 days
Time frame: 24 hours
Melatonin and cortisol pattern (peak times of the levels, dim light melatonin onset) will be assessed from 24 hour blood sampling
Contact information is provided by the study sponsor or research team.
University of Illinois at Chicago
Other
Sleep and Circadian Regulation in Diabetic Retinopathy: The Role of Intrinsically Photosensitive Retinal Ganglion Cells and Melatonin Supplementation
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.
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