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Association Between Plasma Melatonin and No-reflow

Association Between Plasma Melatonin and No-reflow

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03306303
Enrollment
1700
Registered
2017-10-11
Start date
2014-01-01
Completion date
2017-10-01
Last updated
2017-10-11

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

Conditions

ST-segment Elevation Myocardial Infarction

Keywords

melatonin, STEMI, No-reflow

Brief summary

ST-segment elevation myocardial infarction (STEMI) is an acute manifestation of coronary heart disease, remaining a frequent cause of death. A better understanding of risk factors and pathogenic mechanisms underlying STEMI may help improve the prognosis and life quality of these patients. Melatonin is the chief indoleamine produced by the pineal gland, and a well-known antioxidant and free radical scavenger. Basic studies have showed that melatonin is associated with myocardial infarction and heart failure. However, no study has evaluated whether melatonin is associated with adverse clinical outcomes in STEMI patients.

Interventions

None listed

Sponsors

Chinese PLA General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

a diagnosis of STEMI and needed PCI

Exclusion criteria

patients with cancer patients who used melatonin

Design outcomes

Primary

MeasureTime frameDescription
a change in the prevalence of no-reflowmediately after percutaneous coronary intervention (PCI)Thrombolysis in myocardial infarction (TIMI) flow grade of \<3 with a myocardial blush grade of 0-1 was defined as angiographic no-reflow

Secondary

MeasureTime frameDescription
in-hospital complicationsup to 2 weeks after PCIdefined as acute heart failure, atrial fibrillation, chest pain or recurrence of myocardial infarction, complete atrioventricular block, cerebrovascular disease, ventricular fibrillation or ventricular tachycardia
in-hospital major adverse cardiac or cerebrovascular eventsup to 2 weeks after PCIthe composite of death, nonfatal MI, or stroke

Outcome results

None listed

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