An observational study in Acute Coronary Syndrome, sponsored by Peking University First Hospital. Status unknown at 1 site in China. Per ClinicalTrials.gov, last updated 2021-04-27.
Sponsored by Peking University First Hospital · Observational
This is a retrospective, observational, descriptive study which will include patients hospitalized for acute coronary syndrome (ACS) and treated with ticagrelor at discharge. Participants will come from the follow-up program of ACS patients taking ticagrelor 90 mg twice a day as part of the dual antiplatelet therapy at discharge. The primary objectives were to describe the ticagrelor treatment patterns-Ticagrelor persistence, discontinuation, switching, interruption and reasons in Chinese ACS patients; and also to describe 1-year clinical outcomes (Composite of any cause death, myocardial infarction, and stroke) of Chinese ACS patients in real-life practice based on ACS patient follow-up program database.
Background: There are at least 2.5 million acute coronary syndromes (ACS) patients in China per year. Limited data about long term ticagrelor treatment patterns and clinical outcomes in Chinese ACS patients due to the lack of large high quality follow up database. This study is based on real-life practice and ticagrelor is prescribed according to the Chinese guideline and it takes place in real life.
Objective of this study:
Primary Objectives:
Secondary Objectives:
Exploratory Objectives:
To explore the influence factors (age, region, education, insurance, event, etc.) with ticagrelor treatment pattern; Analysis of other possible factors (such as smoke, low density lipoprotein-chlesterol [LDL-C]) affecting the prognosis of patients with ACS; Analysis of possible interactions and their influences between different factors associated with the prognosis of patients with ACS
Study design:
This is a retrospective, observational, descriptive study which will include patients hospitalized for ACS and treated with ticagrelor at discharge.
Data source:
Study participants: Participants will come from the follow-up program of ACS patients taking ticagrelor 90 mg twice a day as part of the dual antiplatelet therapy at discharge. During the follow-up period for 12 months after discharge. Telephone follow-up will be done 1, 3, 6, 12 months after discharge according to a structured questionnaire assessing the primary and secondary objectives of this study. Telephone interviews will be performed by the local ACS patient follow-up program assistants (nurses who enters information in the websites).
Study Variables:
Primary variables:
Secondary variables:
Exploratory variables:
Association between ticagrelor persistence and risk factors (regions, education, reimbursement, etc.); Analysis of other possible factors (such as smoke, LDL-C, etc) affecting the prognosis of patients with ACS; Analysis of possible interactions and their influences between different factors associated with the prognosis of patients with ACS
Exposures of Interest:
Ticagrelor 90 mg used twice a day as part of dual antiplatelet therapy (DAPT) during first year after ACS
Outcomes of Interest:
Limitations:
The study subjects are patients under ticagrelor treatment at discharge in China, which limits the generalization of the study results. The criteria for patients treated with ticagrelor might lead to patient selection bias. As some risk factors of cardiovascular disease (CVD) were not randomized, there might be unmeasured confounding.
1,461 studies on the registry are indexed under Acute Coronary Syndrome; 267 are open to participants now.
This study's planned enrollment of 20,000 is above the median of 500 across 561 observational studies indexed under Acute Coronary Syndrome.
Browse Acute Coronary Syndrome studies →Peking University First Hospital is the lead sponsor of 378 studies on the registry; 178 are open to participants now.
Counted across the registry records on this site, refreshed daily.
ACS patients taking ticagrelor 90 mg twice a day as part of the dual antiplatelet therapy at discharge
Exclusion Criteria:
Patients participated in other interventional clinical trials
Ticagrelor persistence
Duration of ticagrelor treatment: Proportion of patients receiving ticagrelor each month after discharge; Duration from the start of treatment to the end of treatment.
Time frame: 12 months
Ticagrelor discontinuation and reasons for discontinuation
Percentage of patients with ticagrelor discontinuation and related causes: Discontinuation was defined as stopping P2Y12 for at least 3 months.
Time frame: 12 months
Ticagrelor switch and reasons for switching
Percentage of patients with ticagrelor change and related causes: Switching refers to switching from ticagrelor/clopidogrel to another P2Y12 inhibitor (switching from clopidogrel to ticagrelor is a redressing, if documented)
Time frame: 12 months
Ticagrelor interruption and reasons for interruption
Percentage of patients with ticagrelor interruption and related causes: Interruptionn was defined as drug withdrawal for more than 1 day and less than 3 months.
Time frame: 12 months
Major Adverse Cardiovascular Events
Time to the first occurence of Any cause death, myocardial infarction, or Stroke
Time frame: 12 months
Any cause death
Time to the occurence of Any cause death
Time frame: 12 months
Myocardial infarction
Time to the first occurence of Myocardial infarction
Time frame: 12 months
Stroke
Time to the first occurence of Stroke
Time frame: 12 months
Plan to share: No
This study is status unknown, as verified in Apr 2021. You cannot join it, but the record below documents what was studied.
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Peking University First Hospital