Melatonin on Coronary Artery Calcification (MelonCAC)
Primary Purpose
Coronary Artery Calcification
Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Melatonin 3 mg
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Coronary Artery Calcification focused on measuring melatonin, coronary artery calcification, adjuvant therapy
Eligibility Criteria
Inclusion Criteria:
Patients with a documented Agatston score≥30 and moderate calcified coronary atherosclerosis (<50% diameter lumen narrowing) were eligible for the study.
Exclusion Criteria:
- unstable angina pectoris
- symptomatic chronic heart failure and/or left ventricular ejection fraction (EF) <40%
- atrial fibrillation or other arrhythmias
- type I diabetes mellitus or uncontrolled type II diabetes mellitus
- renal failure
- liver disease
- gastrointestinal disease that affected absorption
Sites / Locations
- PLA general hospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Melatonin group
Control group
Arm Description
drug: melatonin tablets (Sigma-Aldrich Co. LLC, St. Louis, MO, USA); the frequency:3mg melatonin tablet was taken daily; duration: study treatment was maintained for 6 months.
drug: placebo tablet; the frequency: placebo tablet was taken daily; duration: study treatment was maintained for 6 months.
Outcomes
Primary Outcome Measures
a change in CAC score at 6 months measured by coronary CTA
The primary efficacy endpoint was the effect of melatonin on the change in CAC score at 6 months compared with placebo.
Secondary Outcome Measures
high-sensitivity C-reactive protein (hsCRP) level
a change in high-sensitivity C-reactive protein (hsCRP) level at 6 months after treatment.
malondialdehyde (MDA) level
a change in malondialdehyde (MDA) level at 6 months after treatment.
Full Information
NCT ID
NCT03966235
First Posted
May 26, 2019
Last Updated
May 28, 2019
Sponsor
Chinese PLA General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03966235
Brief Title
Melatonin on Coronary Artery Calcification
Acronym
MelonCAC
Official Title
Effects of Melatonin on Progression of Coronary Artery Calcification
Study Type
Interventional
2. Study Status
Record Verification Date
May 2019
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2019 (Anticipated)
Primary Completion Date
June 1, 2021 (Anticipated)
Study Completion Date
June 1, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese PLA General Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
5. Study Description
Brief Summary
We planned to evaluate the effects of melatonin on progression of coronary artery calcification (CAC) in patients with moderate calcified coronary atherosclerosis.
Detailed Description
CAC is prevalent in coronary artery disease (CHD), and the extent of CAC predicts cardiovascular risk. The causes of CAC include dysregulated matrix metabolism, epitaxial mineral deposition, inflammation, oxidative stress, and apoptosis. Melatonin is the main indoleamine produced by the pineal gland; it is known recently to have anti-inflammatory, anti-cancer and antioxidant activities. Several studies have shown that melatonin protects against inflammation and apoptosis in vascular calcification. Melatonin also inhibits oxidative stress-induced apoptosis and calcification in endplate chondrocytes. The investigators planned to determine the efficacy of melatonin on progression of coronary artery calcification (CAC) in patients with moderate calcified coronary atherosclerosis. This study may shed light as to whether oral melatonin supplementation can be an adjunct therapy in CAC patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Calcification
Keywords
melatonin, coronary artery calcification, adjuvant therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
74 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Melatonin group
Arm Type
Experimental
Arm Description
drug: melatonin tablets (Sigma-Aldrich Co. LLC, St. Louis, MO, USA); the frequency:3mg melatonin tablet was taken daily; duration: study treatment was maintained for 6 months.
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
drug: placebo tablet; the frequency: placebo tablet was taken daily; duration: study treatment was maintained for 6 months.
Intervention Type
Drug
Intervention Name(s)
Melatonin 3 mg
Other Intervention Name(s)
melatonin
Intervention Description
Melatonin was taken daily for 6 months.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo tablet was taken daily for 6 months.
Primary Outcome Measure Information:
Title
a change in CAC score at 6 months measured by coronary CTA
Description
The primary efficacy endpoint was the effect of melatonin on the change in CAC score at 6 months compared with placebo.
Time Frame
at 6 months
Secondary Outcome Measure Information:
Title
high-sensitivity C-reactive protein (hsCRP) level
Description
a change in high-sensitivity C-reactive protein (hsCRP) level at 6 months after treatment.
Time Frame
at 6 months
Title
malondialdehyde (MDA) level
Description
a change in malondialdehyde (MDA) level at 6 months after treatment.
Time Frame
at 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with a documented Agatston score≥30 and moderate calcified coronary atherosclerosis (<50% diameter lumen narrowing) were eligible for the study.
Exclusion Criteria:
unstable angina pectoris
symptomatic chronic heart failure and/or left ventricular ejection fraction (EF) <40%
atrial fibrillation or other arrhythmias
type I diabetes mellitus or uncontrolled type II diabetes mellitus
renal failure
liver disease
gastrointestinal disease that affected absorption
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
wei ren chen, MD
Phone
+8601066876231
Email
chen_weiren@sina.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
yu jie zhou
Organizational Affiliation
Beijing Anzhen Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
PLA general hospital
City
Beijing
ZIP/Postal Code
100853
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
wei ren chen
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30476723
Citation
Gilham D, Tsujikawa LM, Sarsons CD, Halliday C, Wasiak S, Stotz SC, Jahagirdar R, Sweeney M, Johansson JO, Wong NCW, Kalantar-Zadeh K, Kulikowski E. Apabetalone downregulates factors and pathways associated with vascular calcification. Atherosclerosis. 2019 Jan;280:75-84. doi: 10.1016/j.atherosclerosis.2018.11.002. Epub 2018 Nov 14.
Results Reference
background
PubMed Identifier
28122774
Citation
Shobeiri N, Bendeck MP. Interleukin-1beta Is a Key Biomarker and Mediator of Inflammatory Vascular Calcification. Arterioscler Thromb Vasc Biol. 2017 Feb;37(2):179-180. doi: 10.1161/ATVBAHA.116.308724. No abstract available.
Results Reference
background
PubMed Identifier
26201382
Citation
Fernandez A, Ordonez R, Reiter RJ, Gonzalez-Gallego J, Mauriz JL. Melatonin and endoplasmic reticulum stress: relation to autophagy and apoptosis. J Pineal Res. 2015 Oct;59(3):292-307. doi: 10.1111/jpi.12264. Epub 2015 Aug 9.
Results Reference
background
PubMed Identifier
29203148
Citation
Dehdashtian E, Mehrzadi S, Yousefi B, Hosseinzadeh A, Reiter RJ, Safa M, Ghaznavi H, Naseripour M. Diabetic retinopathy pathogenesis and the ameliorating effects of melatonin; involvement of autophagy, inflammation and oxidative stress. Life Sci. 2018 Jan 15;193:20-33. doi: 10.1016/j.lfs.2017.12.001. Epub 2017 Dec 5.
Results Reference
background
PubMed Identifier
26681403
Citation
Wang Z, Ni L, Wang J, Lu C, Ren M, Han W, Liu C. The protective effect of melatonin on smoke-induced vascular injury in rats and humans: a randomized controlled trial. J Pineal Res. 2016 Mar;60(2):217-27. doi: 10.1111/jpi.12305. Epub 2016 Jan 13.
Results Reference
result
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Melatonin on Coronary Artery Calcification
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