NCT02099422

Brief Summary

Comparison of two antiplatelet strategies between months 1 and 12 after coronary stenting for ACS. Efficiency and tolerance évaluation

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2013

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
unknown

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, 2013

Completed
1.2 years until next milestone

First Submitted

Initial submission to the registry

March 26, 2014

Completed
2 days until next milestone

First Posted

Study publicly available on registry

March 28, 2014

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2015

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2016

Completed
Last Updated

March 28, 2014

Status Verified

March 1, 2014

Enrollment Period

2 years

First QC Date

March 26, 2014

Last Update Submit

March 26, 2014

Conditions

Acute Coronary SyndromeCoronary StentingAntiplatelet Therapy

Outcome Measures

Primary Outcomes (1)

  • combined ischemic and hemorragic endpoint

    12 months

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with ACS treated by coronary stent implantation

You may qualify if:

  • ACS and coronary stenting one month ago

You may not qualify if:

  • age under 18 and pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU Timone hospital . Sc CARDIOLOGIE. Rue saint Pierre.

Marseille, 13005, France

RECRUITING

MeSH Terms

Conditions

Acute Coronary Syndrome

Condition Hierarchy (Ancestors)

Myocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular Diseases

Central Study Contacts

thomas cuisset, MD-PHD

CONTACT

33(0) 491385981thomas.cuisset@ap-hm.fr

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD-PHD

Study Record Dates

First Submitted

March 26, 2014

First Posted

March 28, 2014

Study Start

January 1, 2013

Primary Completion

January 1, 2015

Study Completion

January 1, 2016

Last Updated

March 28, 2014

Record last verified: 2014-03

Locations

FR(1)