NCT01075867

Brief Summary

To demonstrate the effectiveness of the ELIPS programme (Multi-dimEnsionaL preventIon Program after Acute coronary Syndrome), which aims at improving quality of care of patients admitted to hospital with Acute Coronary Syndrome (ACS) in the Swiss setting. The program targets an increase in prescription rates by physicians and long term medication adherence and adoption of healthy lifestyle attitudes by patients. The program is dedicated to caregivers to increase their application of guidelines into practice, to increase their confidence in therapeutic education of patients, and to patients to improve their understanding of ACS and its treatment and to increase their motivation for long term treatment,.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
2,498

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Apr 2010

Longer than P75 for all trials

Geographic Reach
1 country

4 active sites

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

First Submitted

Initial submission to the registry

February 24, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

February 25, 2010

Completed
1 month until next milestone

Study Start

First participant enrolled

April 1, 2010

Completed
3.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2013

Completed
5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2018

Completed
Last Updated

April 30, 2020

Status Verified

April 1, 2020

Enrollment Period

3.7 years

First QC Date

February 24, 2010

Last Update Submit

April 28, 2020

Conditions

Outcome Measures

Primary Outcomes (1)

  • composite of death and cardiovascular event

    Composite of * death from any cause, * myocardial infarction, * documented unstable angina requiring rehospitalization, * revascularization (performed at least 30 days after randomization), * documented new or worsen lower limb ischemia, * stroke * transient cerebral ischemic accident.

    1 year

Secondary Outcomes (3)

  • Process outcome at discharge

    1 year

  • Clinical outcomes at follow-up

    1 year

  • Surrogate outcomes at follow-up

    1 year

Study Arms (2)

Control group

Before ELIPS implementation 12 months follow-up

Treatment group

After ELIPS implementation 12 months follow-up

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients Admitted for an Acute Coronary Syndrome

You may qualify if:

  • Patients \>18 years
  • Admitted for an ACS, that is with symptoms compatible with angina pectoris (chest pain, breathlessness) and at least one of the following 3 features : a) Elevation or depression of the ST segment, inverted T waves or dynamic changes in the repolarization phase b) Positive troponin c) Known coronary artery disease. A significant coronary artery disease must be confirmed angiographically.

You may not qualify if:

  • Severe physical disability or dement
  • Less than 1 year of life expectancy for non cardiac reason

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (4)

University Hospital

Bern, Switzerland

Location

University Hospitals

Geneva, Switzerland

Location

University Hospital

Lausanne, Switzerland

Location

University Hospital,

Zurich, Switzerland

Location

Related Publications (1)

  • Weidmann L, Obeid S, Mach F, Shahin M, Yousif N, Denegri A, Muller O, Raber L, Matter CM, Luscher TF. Pre-existing treatment with aspirin or statins influences clinical presentation, infarct size and inflammation in patients with de novo acute coronary syndromes. Int J Cardiol. 2019 Jan 15;275:171-178. doi: 10.1016/j.ijcard.2018.10.050. Epub 2018 Oct 16.

Related Links

MeSH Terms

Conditions

Acute Coronary Syndrome

Condition Hierarchy (Ancestors)

Myocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Pr

Study Record Dates

First Submitted

February 24, 2010

First Posted

February 25, 2010

Study Start

April 1, 2010

Primary Completion

December 1, 2013

Study Completion

December 1, 2018

Last Updated

April 30, 2020

Record last verified: 2020-04

Locations