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The multicenter clinical trials of the IV phase of acute ST segment elevation myocardial infarction treated with recombinant human urokinase (Pu Youke)

The clinical trial of IV phase of acute ST segment elevation myocardial infarction treated with recombinant human urokinase (Pu Youke) injection

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIN-16008125
Enrollment
Unknown
Registered
2016-03-21
Start date
2012-06-01
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 ST segment elevation myocardial infarction

Interventions

Intervention gro:Intravenous administration of recombinant human urokinase (Pu Youke)

Sponsors

The Second Hospital Affiliated to Tianjin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) severe persistent chest pain more than 30 minutes or more, can not alleviate the symptoms; (2) 2 adjacent or above 2 ST elevation, in limb leads more than 0.lmV, more than 0.2mV chest lead; (3) the proposed on to thrombolysis time less than 6 hours; (4) 18-75 years old, aged above 75 years old unable to accept PCI, as appropriate, the use of reduction; (5) patients / or their families are willing to take part in this experiment agree to sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) currently in use of anticoagulants; (2) there is a history of bleeding, trauma, internal organs (including biopsy) in a month, or at present, there is an active peptic ulcer disease; (3) with traumatic cardiopulmonary resuscitation (traumatic CPR is equal to or more than 10 minutes), 2 weeks had not implementation of the compressed blood vessel puncture had a history of trauma; (4) in patients with essential hypertension after active antihypertensive therapy, blood pressure is greater than or equal to 180/110mmHg persons (tolic blood pressure, diastolic blood pressure either one reached the standard for blood pressure); (5) suspected aortic dissection, infective endocarditis, can not be excluded the preceding diagnosis; (6) cardiac shock or severe left heart failure pulmonary edema after expansion use of vasoactive drugs; (7) previous cerebral hemorrhage, hemorrhagic stroke, or subarachnoid hemorrhage. There are other stroke or cerebral vascular events (including TIA), known intracranial tumors, cerebral vascular malformations in 6 months; (8) there is a bleeding retinal history; (9) a variety of hematologic diseases, bleeding disorders or bleeding tendencies; (10) patients with severe liver kidney dysfunction, severe depletion of state, or malignancy; (11) female pregnancy; (12) patients / or their families are not willing to take part in this experiment, not willing to sign the informed consent; (13) doctors believe that other conditions are not suitable for intravenous thrombolysis.

Design outcomes

Primary

MeasureTime frame
Clinical opening rate;Coronary patency rate;

Countries

China

Contacts

Public ContactLi Guangping

The Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine

liguang@163.com+86 022-28331788

Outcome results

None listed

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