Viewing Study NCT01088503



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Last Modification Date: 2024-10-26 @ 10:17 AM
Study NCT ID: NCT01088503
Status: COMPLETED
Last Update Posted: 2016-01-29
First Post: 2010-03-15

Brief Title: Treatment With Adenosine Diphosphate ADP Receptor Inhibitors Longitudinal Assessment of Treatment Patterns and Events After Acute Coronary Syndrome
Sponsor: Eli Lilly and Company
Organization: Eli Lilly and Company

Study Overview

Official Title: The TRANSLATE-ACS Study Treatment With ADP Receptor Inhibitors Longitudinal Assessment of Treatment Patterns and Events After Acute Coronary Syndrome
Status: COMPLETED
Status Verified Date: 2015-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: TRANSLATE-ACS
Brief Summary: The TReatment with ADP receptor iNhibitorS Longitudinal Assessment of Treatment Patterns and Events after Acute Coronary Syndrome TRANSLATE-ACS study is a prospective observational longitudinal study to evaluate the real world effectiveness and use of prasugrel and other ADP receptor inhibitor therapies among myocardial infarction MI participants treated with percutaneous coronary intervention PCI during the index hospitalization Participant management and treatment decisions are at the discretion of the care team per routine clinical practice Approximately 17000 participants will be enrolled at approximately 350 sites in the United States Follow-up will be conducted through 15 months in approximately 15650 participants

TRANSLATE-ACS will complement the results of both randomized controlled clinical trials and current registries in addressing the real world treatment patterns and clinical outcomes for MI participants managed with PCI and initiated on ADP receptor inhibitor therapy In addition to determining the effectiveness of prasugrel in comparison to other ADP receptor inhibitors the study will also determine factors associated with initial ADP receptor inhibitor selection and longitudinal patterns of use evaluate the safety and describe and compare resource use and medical costs associated with ADP receptor inhibitors Additionally this study will generate a continuum of information from the inpatient to outpatient settings to provide a comprehensive picture of participant treatment and outcomes not currently available for novel ADP receptor inhibitors
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
H7T-US-B007 OTHER Eli Lilly and Company None