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UnknownNCT03137212

Safety and Efficacy of Percutaneous Coronary Intervention Combined With Thrombolysis at Different Time

Study of Safety and Efficacy of Percutaneous Coronary Intervention Combined With Thrombolysis by Recombinant Human Prourokinase at Different Time

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Second Hospital of Jilin University · Academic / Other
Sex
All
Age
19 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Patients with acute ST-segment elevation myocardial infarction and thrombolysis indications, will be given the recombinant human prourokinase for thrombolysis treatment, and in accordance with the guidelines, will be treated with coronary angiography examination 3 to 24 hours after thrombolysis. The study will explore the best time for interventional therapy combined with thrombolysis.

Detailed description

The noninferiority multicenter, prospective, randomized, controlled study of urokinase of restructuring the original design evaluation (rhPro - UK) at different times after thrombolysis combined with percutaneous coronary intervention(PCI)therapy of acute ST segment elevation myocardial infarction.Patients with acute ST segment elevation myocardial infarction and thrombolysis indications, will be given the recombinant human prourokinase for thrombolysis treatment, and in accordance with the guidelines, will be treated with coronary angiography examination 3 to 24 hours after thrombolysis. The study will explore the best time for interventional therapy combined with thrombolysis.

Conditions

Interventions

TypeNameDescription
COMBINATION_PRODUCTthrombolysis and PCI of A typeSTEMI patients first are given thrombolysis and then transfer to PCI centers to be treated by PCI 3-6 hours after thrombolysis.
COMBINATION_PRODUCTthrombolysis and PCI of B typeSTEMI patients first are given thrombolysis and then transfer to PCI centers to be treated by PCI 6-24 hours after thrombolysis.

Timeline

Start date
2017-04-17
Primary completion
2020-03-31
Completion
2020-03-31
First posted
2017-05-02
Last updated
2017-05-02

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03137212. Inclusion in this directory is not an endorsement.