Remote Ischemic Postconditioning Percutaneous Coronary Intervention Randomized Trial

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-14005114

Enrollment

Unknown

Registered

2014-08-18

Start date

2014-08-20

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

acute myocardial infarction

Interventions

Control group:PCI

RIPC1:5'*5'*3RIPC

RIPC2:5'*5'*3 Early RIPC

RIPC3:2'*2'*3RIPC

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ST segment elevation myocardial infarction patients;For stable angina or unstable angina angiography or PCI surgery patients.

Exclusion criteria

Exclusion criteria: In PCI before 4 weeks, increased troponin in patients with myocardial infarction; 1. heart failure (NYHA III or IV); Chronic inflammatory diseases (such as lupus erythematosus, rheumatoid arthritis). Severe kidney damage (glomerular filtration rate 50 mm) With glyburide (ATP potassium channel blockers, influence ischemic conditioning effect).

Design outcomes

Primary

Measure	Time frame
CK;CK-MB;troponin;cardiac uhrasonography;MUGA;BR;blood biochemical;renal function;electrocardiogram;Limb doppler;blood pressur;	—

Countries

China

Contacts

Public ContactYang Yining

yangyn5126@163.com+86 13199860611

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026