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Long-term MOno-Antiplatelet Drug Strategy After PerCutanEous CoronAry InterveNtion

NCT03725800 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2018-10-31

No results posted yet for this study

Summary

The OCEAN (long-term mOn-antiplatelet drug strategy after perCutanEous coronANy intervention) study is the largest prospective multicenter data base to investigate the long-term incidence and prognosis of the use of agents for antiplatelet-induced GI injury symptoms (AI-GIS) or GI hemorrhage among patients undergoing PCI. The OCEAN study will provide evidence of the long-term incidence and prognosis of use of agents for AI-GIS among patients undergoing PCI. It has the potential to provide an optimal long-term mono-antiplatelet strategy.

Conditions

  • Antiplatelet Drug-related Gastrointestinal Injury

Sponsors & Collaborators

  • Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

    collaborator OTHER

  • The First Affiliated Hospital of Guangdong Pharmaceutical University

    collaborator OTHER

  • Guangzhou Panyu Central Hospital

    collaborator OTHER

  • First People's Hospital, Shunde China

    collaborator OTHER

  • Second People's Hospital of Foshan City

    collaborator UNKNOWN

  • The First People's Hospital of Qingyuan

    collaborator UNKNOWN

  • Zhongshan People's Hospital, Guangdong, China

    collaborator OTHER

  • Huadu District People's Hospital of Guangzhou

    collaborator OTHER

  • Guangdong Provincial People's Hospital

    lead OTHER

Principal Investigators

  • Yong Liu, MD,PhD · Guangdong Cardiovascular Institute,Guangdong General Hospital

  • Shiqun Chen, MS · Guangdong Cardiovascular Institute,Guangdong General Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-10-15
Primary Completion
2019-10-31
Completion
2019-11-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03725800 on ClinicalTrials.gov