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Characteristics of biomarker on dermal sensitization for myocardial ischemia-reperfusion injury

Characteristics of biomarker on dermal sensitization for myocardial ischemia-reperfusion injury

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2024000180
Enrollment
Unknown
Registered
2024-08-07
Start date
2024-08-31
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

myocardial ischemia reperfusion injury

Interventions

conductive sensitization
MIRI group:morphological sensitization
healthy group:morphological sensitization
algetic sensitization
pyretic sensitization
conducive sensitization

Sponsors

the Affiliated Hospital of Shaanxi University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: MIRI patients: (1) meeting the diagnostic criteria of non-ST elevation acute coronary syndrome in 2023 ESC Guidelines for the management of acute coronary syndromes. (2) received percutaneous coronary intervention within a week. (3) aged 18 to 85 years. (4) willing to participate in this study, and sign on informed consent. Healthy subjects: (1) received a health examination within a week, and confirmed to be in good health. (2) aged 18 to 85 years, and matching the MIRI patients. (3) willing to participate in this study, and sign on informed consent.

Exclusion criteria

Exclusion criteria: (1) diagnosed as ST-elevation myocardial infarction, with persistent ST-segment elevation or ST-segment elevation equivalents on electrocardiogram. (2) combined with disorders of rhythm, disorders of the heart, muscles, valves, and pericardium, and peripheral vascular disease. (3) suffering from neoplastic disorders, hematopoietic disorders, disorders of hemostasis, infectious diseases, immune-mediated, inflammatory, and rheumatologic disorders. (4) combined with fever. (5) suffering from psychiatric disorders, and unable to cooperate. (6) participating in any other study using an unapproved drug within 3 months.

Design outcomes

Primary

MeasureTime frame
mRNA;

Countries

China

Contacts

Public ContactHaifa Qiao

College of Acupuncture and Tuina, Shaanxi University of Chinese Medicine

1511006@sntcm.edu.cn18220046518

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026