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Melatonin Supplementation to Improve Sleep in Patients With Heart Failure

Primary Purpose

Heart Failure, Sleep Disorders

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
melatonin
placebo
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring 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

Eligibility Criteria

35 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Brigham and Women's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

melatonin

placebo

Arm Description

melatonin

placebo

Outcomes

Primary Outcome Measures

Change in sleep quantity assessed by actigraphy

Secondary Outcome Measures

Change in quality of life and heart failure biomarkers

Full Information

First Posted
March 25, 2009
Last Updated
January 17, 2018
Sponsor
Brigham and Women's Hospital
Collaborators
American Academy of Sleep Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT00869869
Brief Title
Melatonin Supplementation to Improve Sleep in Patients With Heart Failure
Official Title
Restoration of Sleep in Heart Failure Patients
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Withdrawn
Why Stopped
No subjects were enrolled in this study. Funding ran out.
Study Start Date
March 2009 (undefined)
Primary Completion Date
March 2010 (Anticipated)
Study Completion Date
March 2011 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
Collaborators
American Academy of Sleep Medicine

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
melatonin
Arm Type
Experimental
Arm Description
melatonin
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo
Intervention Type
Drug
Intervention Name(s)
melatonin
Intervention Description
2.5 mg melatonin, by mouth, 1 per day, for 3-4 weeks
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo
Primary Outcome Measure Information:
Title
Change in sleep quantity assessed by actigraphy
Time Frame
measured during ambulatory phase
Secondary Outcome Measure Information:
Title
Change in quality of life and heart failure biomarkers
Time Frame
measured during study visits

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frank A.J.L. Scheer, Ph.D.
Organizational Affiliation
Brigham and Women's Hospital, Harvard Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
14732734
Citation
Scheer FA, Van Montfrans GA, van Someren EJ, Mairuhu G, Buijs RM. Daily nighttime melatonin reduces blood pressure in male patients with essential hypertension. Hypertension. 2004 Feb;43(2):192-7. doi: 10.1161/01.HYP.0000113293.15186.3b. Epub 2004 Jan 19.
Results Reference
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PubMed Identifier
15649734
Citation
Scheer FA, Czeisler CA. Melatonin, sleep, and circadian rhythms. Sleep Med Rev. 2005 Feb;9(1):5-9. doi: 10.1016/j.smrv.2004.11.004. No abstract available.
Results Reference
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PubMed Identifier
16130027
Citation
Scheer FA, Zeitzer JM, Ayas NT, Brown R, Czeisler CA, Shea SA. Reduced sleep efficiency in cervical spinal cord injury; association with abolished night time melatonin secretion. Spinal Cord. 2006 Feb;44(2):78-81. doi: 10.1038/sj.sc.3101784.
Results Reference
background
PubMed Identifier
16364835
Citation
Scheer FA. Potential use of melatonin as adjunct antihypertensive therapy. Am J Hypertens. 2005 Dec;18(12 Pt 1):1619-20. doi: 10.1016/j.amjhyper.2005.07.013. No abstract available.
Results Reference
background
PubMed Identifier
17533214
Citation
Scheer FA, Stone PH, Shea SA. Decreased sleep in heart failure: are medications to blame? Arch Intern Med. 2007 May 28;167(10):1098-9; author reply 1099-100. doi: 10.1001/archinte.167.10.1098-b. No abstract available.
Results Reference
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Melatonin Supplementation to Improve Sleep in Patients With Heart Failure

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