Skip to content

A cross-sectional study on the characteristics and distribution of acupoint sensitization in patients with myocardial reperfusion injury after cardiac stenting

A cross-sectional study on the characteristics and distribution of acupoint sensitization in patients with myocardial reperfusion injury after cardiac stenting

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2024000107
Enrollment
Unknown
Registered
2024-06-23
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-07-23

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

None listed

Sponsors

Shaanxi University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: MIRI Group: (1) Meet the diagnostic criteria of the European Society of Cardiology Guidelines 2023 for non-ST elevation acute coronary syndromes; (2) PCI and implantation of at least one stent within one week; (3) Race, gender, age =18 years old, < 85 years old; (4) Voluntarily participate in the study and sign the informed consent. Healthy subject group (1) Healthy body, no cardiovascular system disease, no mental disease; (2) Race, gender, age =18 years old, < 85 years old; (3) Voluntarily participate in the study and sign the informed consent. Note: Only those who meet the above criteria can be included in this study.

Exclusion criteria

Exclusion criteria: MIRI Group: (1) In STEMI patients, the ECG showed continuous ST segment elevation (at least two consecutive ST segment elevations from point J: ?V2 to V3 leads =2.5mm, male < 40 years old, or =2mm, male =40 years old, or =1.5mm, female no age; (2) Other leads =1mm, except left ventricular hypertrophy or left bundle branch block; ? Right chest lead V3R ~ V4R, or back lead V7 ~ V9=0.5mm); (2) Suffering from malignant tumors, severe infectious diseases, inflammatory diseases, autoimmune diseases, blood system diseases, acute cerebral infarction; (3) Patients with bullosa skin disease, granulomatous skin disease, metabolic skin disease, and connective tissue disease that are difficult to diagnose clinically; (4) Participate in any other drug study or treatment study using an unapproved drug within the previous 3 months; (5) Pregnant and lactating women; (6) suffering from mental illness or accompanied by serious psychological disorders, unable to cooperate; Note: Patients who meet any 1 of the above criteria will be excluded. Healthy subjects Group: (1) Anxiety, depression, cognitive disabilities, allergies; (2) Pregnant and lactating women; (3) Participants in other clinical trials. Note: Patients who meet any 1 of the above criteria will be excluded.

Design outcomes

Primary

MeasureTime frame
The skin change shape;Skin temperature; Value of resistance;Tenderness threshold;

Countries

China

Contacts

Public ContactQiao haifa

Shaanxi University of Traditional Chinese Medicine

1511006@sntcm.edu.cn18220046518

Outcome results

None listed

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