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NCT Number: NCT04547439

Sleep, Diabetic Retinopathy and Melatonin

This study explores the use of melatonin in patients with diabetic retinopathy

Recruiting

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Key information

Age range

40 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of Illinois at Chicago

Chicago, Illinois, 60612, United States

Location status: Recruiting

Location contact

Sirimon Reutrakul, MD

CONTACT

About this study

This is a randomized controlled study using melatonin for 8 weeks in patients with diabetic retinopathy on outcomes of sleep and circadian regulation

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Type 2 diabetes (clinically diagnosed, taking anti-diabetes medications or history of elevated A1C≥6.5%)
  • 40-65 years of age
  • Diabetic retinopathy of at least moderate degree

Exclusion criteria

  • use of melatonin
  • antidepressants or antipsychotics
  • illicit drug use
  • night shift work or travel beyond 2 time zones in the month before enrollment
  • end stage renal disease requiring renal replacement therapy
  • history of stroke or transient ischemic attacks
  • history of dementia or memory impairment
  • uncontrolled congestive heart failure or recent hospitalization for cardiac condition (6 months)
  • chronic obstructive pulmonary disease requiring oxygen
  • severe chronic liver disease such as cirrhosis
  • ongoing treatment for major medical problems such as cancer
  • history of severe hypoglycemia defined as hypoglycemic episodes requiring assistance from others within the past six months.
  • Significant depressive symptoms
  • untreated severe OSA (AHI≥ 30 events/hour),
  • uncontrolled hypertension (blood pressure ≥ 160/100 mmHg),
  • uncontrolled diabetes (A1C ≥ 11%),
  • abnormal TSH
  • abnormal liver function (AST or ALT>3x upper limits of normal
  • use of sedatives and hypnotics.
  • clinically significant epiretinal membranes, clinically significant lens opacities, or cystoid macular edema, iris neovascularization, iris atrophy, or an asymmetrically shaped pupil, nuclear sclerotic, posterior subcapsular, or cortical lens opacities greater than 2+, a history of pan-retinal photocoagulation.
  • hemoglobin <11.5 g/dL in women and <13.5 g/dL in men.

Treatment and study plan

Melatonin

Drug

Melatonin 3 mg will be taken nightly for 8 weeks

Placebo

Other

Placebo will be given nightly for 8 weeks

Primary outcomes

  1. Sleep pattern

    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

  2. Melatonin and Cortisol Rhythm

    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

Study contacts

Contact information is provided by the study sponsor or research team.

Sirimon Reutrakul

CONTACT

[email protected]

3129966060

Sponsors and collaborators

Lead sponsor

University of Illinois at Chicago

Other

Collaborators

  • University of Chicago

Registry information

Official study title

Sleep and Circadian Regulation in Diabetic Retinopathy: The Role of Intrinsically Photosensitive Retinal Ganglion Cells and Melatonin Supplementation

Important dates

Study start
2021
Primary completion
2026
Study completion
2026
First posted
Sep 14, 2020
Registry last updated
Apr 21, 2026

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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