NCT02576691

Brief Summary

The purpose of this study is To assess percutaneous coronary intervention 's effect on short- and long- term outcomes, and complication incidence in resuscitated victims of cardiac arrest after acute myocardial infarction

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,363

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2005

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2005

Completed
8.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2013

Completed
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2015

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

October 13, 2015

Completed
2 days until next milestone

First Posted

Study publicly available on registry

October 15, 2015

Completed
Last Updated

October 15, 2015

Status Verified

October 1, 2015

Enrollment Period

8.3 years

First QC Date

October 13, 2015

Last Update Submit

October 14, 2015

Conditions

Acute Myocardial Infarction

Keywords

cardiac arrestpercutaneous coronary interventioncardiogenic shockoutcome

Outcome Measures

Primary Outcomes (1)

  • all cause mortality

    2 years

Study Arms (2)

The PCI group

The PCI group was composed of patients who underwent PCI following the return of spontaneous circulation or after CA.

Device: percutaneous coronary intervention

Non-PCI group

Non-PCI group included patients who didn't undergo PCI or were subjected to PCI before CA

Interventions

percutaneous coronary interventionDEVICE
The PCI group

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

20 million residents of the South of Zhejiang Province

You may qualify if:

  • underwent successful cardiopulmonary resuscitation from CA after AMI

You may not qualify if:

  • late tumor;
  • underwent Coronary Artery Bypass Grafting after CAG;
  • with no attempted resuscitation.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Heart ArrestShock, Cardiogenic

Interventions

Percutaneous Coronary Intervention

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular DiseasesMyocardial InfarctionMyocardial IschemiaVascular DiseasesInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosisShock

Intervention Hierarchy (Ancestors)

Endovascular ProceduresVascular Surgical ProceduresCardiovascular Surgical ProceduresSurgical Procedures, OperativeMinimally Invasive Surgical Procedures

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
First Affiliated Hospital of Wenzhou Medical University, Yuanli Lei

Study Record Dates

First Submitted

October 13, 2015

First Posted

October 15, 2015

Study Start

January 1, 2005

Primary Completion

April 1, 2013

Study Completion

April 1, 2015

Last Updated

October 15, 2015

Record last verified: 2015-10