Heart Failure, Sleep Disorders
Conditions
Keywords
Heart Failure, Sleep Disorders, Melatonin, Antioxidants, Molecular Mechanisms of Pharmacological Action, Nervous System Diseases, Physiological Effects of Drugs, Vascular Diseases, Central Nervous System Depressants, Protective Agents, Pharmacologic Actions, Signs and Symptoms, Mental Disorders, Therapeutic Uses, Neurologic Manifestations, Cardiovascular Diseases, Central Nervous System Agents
Brief summary
The purpose of this study is to determine whether melatonin can improve sleep, quality of life and markers of heart failure in patients with heart failure.
Detailed description
Heart failure affects nearly 5 million individuals in the United States and constitutes a prime risk factor for morbidity and mortality. Beta-blockers are a class of drugs that form a critical part of the best treatment of heart failure, and thereby decrease the risk for these serious problems. Beta-blockers also lower the levels of melatonin, a hormone that has a sleep-promoting effect. Most patients with heart failure take beta-blockers and have poor sleep, which may be related to the beta-blockers' effect on melatonin levels. This study will evaluate the effectiveness of treatment with melatonin supplements in improving sleep in individuals with heart failure who are taking beta-blockers. In addition, the study will examine whether the melatonin supplements aid in improving quality of life and measures of heart failure. Participants in this double-blind study will be randomly assigned to receive either melatonin supplements or placebo for the duration of the study. The study will mainly take place at home, where participants will complete sleep diaries, measure blood pressure and wear a wrist watch that measures movement for 5-6 weeks. During that time there will be three visits to the hospital where plasma and urine samples will be collected and questionnaires will be completed.
Interventions
2.5 mg melatonin, by mouth, 1 per day, for 3-4 weeks
placebo
Sponsors
Study design
Eligibility
Inclusion criteria
* Diagnosed with heart failure NYHA Class 2 or 3 * Currently being treated with beta-blocker
Exclusion criteria
* Diagnosed with obstructive sleep apnea * Using Fluvoxamine, Warfarin, Nifedipine, or Calcium Channel Blockers
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in sleep quantity assessed by actigraphy | measured during ambulatory phase |
Secondary
| Measure | Time frame |
|---|---|
| Change in quality of life and heart failure biomarkers | measured during study visits |
Countries
United States