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Melatonin Supplementation to Improve Sleep in Patients With Heart Failure

Restoration of Sleep in Heart Failure Patients

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00869869
Enrollment
0
Registered
2009-03-26
Start date
2009-03-31
Completion date
2011-03-31
Last updated
2018-01-19

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

Conditions

Heart Failure, Sleep Disorders

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

DRUGmelatonin

2.5 mg melatonin, by mouth, 1 per day, for 3-4 weeks

DRUGplacebo

placebo

Sponsors

American Academy of Sleep Medicine
CollaboratorOTHER
Brigham and Women's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
35 Years to 75 Years
Healthy volunteers
No

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

MeasureTime frame
Change in sleep quantity assessed by actigraphymeasured during ambulatory phase

Secondary

MeasureTime frame
Change in quality of life and heart failure biomarkersmeasured during study visits

Countries

United States

Outcome results

None listed

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