Beta Blocker Interruption After Uncomplicated Myocardial Infarction

Myocardial Infarction Clinical Trial

— AßYSS  

Official title:

Assessment of βeta Blocker Interruption After Uncomplicated mYocardial Infarction on Safety and Symptomatic Cardiac Events Requiring Hospitalization: The AβYSS Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03498066
• Other study ID #: P150946J
• Status: Completed
• Phase: Phase 4
• Start date: August 29, 2018
• Est. completion date: October 31, 2023

Study information

• Verified date: November 2023
• Source: Assistance Publique - Hôpitaux de Paris
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

ABYSS is a national, multicenter, randomised, open label trial using the PROBE study design, that will evaluate the non-inferiority of the interruption of ΒB therapy after an uncomplicated MI after six months or more of follow-up compared to the continuation of βB evaluated by the primary endpoint or death, MI, Stroke and rehospitalization for others cardiovascular reasons.

Description:

Despite the outstanding progress made in cardiac care over the last few years, cardiovascular diseases remain the leading cause of morbidity and mortality in developed countries. After the initial clinical event, patients are considered to have a chronic disease which combined with the increasing actual life expectancy patients with CAD are a major source of expenses due to their life-long treatment and follow-up. ΒB are prescribed during the initial hospitalisation for MI and in the post-MI phase. European (European Society of Cardiology, ESC) and American (ACC/AHA) guidelines initially gave βB therapy a class I recommendation for MI or acute coronary syndrome (ACS) for the first year of treatment and extended such recommendation without solid data up to 3 years after MI , . However, there has been no recent clinical trial to evaluate safety and efficacy of long term ΒB therapy in the contemporary therapeutic era. Taking such lack of evidence in account and acknowledging that clinical practice has changed, the latest ESC STEMI (2014) and NSTEMI (2015) Guidelines degraded the recommendation for the use of ΒB in post MI patients (Class IIa B) during the hospitalization period and they question the validity of its use after the initial stabilization phase. This was confirmed in the 2017 STEMI Guidelines. The primary objective of the ABYSS trial is to demonstrate the non-inferiority of the interruption of ΒB therapy after an uncomplicated MI after six months or more of follow-up compared to the continuation of βB evaluated by the primary endpoint. The primary endpoint of the study will be evaluated, with one-year minimum follow-up, and will be the composite of Major Adverse Cardiovascular Events (MACE) measured at the longest follow-up including: - All-cause death - Stroke - Myocardial infarction Hospitalisation for other cardiovascular (CV) reason. It is expected that the interruption of βB therapy will not alter the prognosis of patients and improve safety and quality of life of patients and considerably reduce healthcare direct or indirect costs.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 3700
• Est. completion date: October 31, 2023
• Est. primary completion date: October 31, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion criteria Subjects meeting all of the following criteria will be considered for enrolment into the

study:

1. Male or female +/=18 years of age

2. Current treatment with ßB whatever the drug or the dose used

3. Prior acute myocardial infarction 6 months or more before randomisation defined either by: AßYSS protocol, version 3.0 of 25/05/2021 Page 32 / 65

• An episode of ST elevation MI with ST segment elevation (STEMI) and/or the presence of Q wave (Type I MI)
• an episode of Non ST Elevation MI (NSTEMI) with preferably at least one of the

followings:

• i) a documented hypokinetic or akinetic segment on echo or any other imaging technique
• ii) segmental hypoperfusion Thallium or any other imaging technique
• iii) segmental aspect of necrosis on MRI
• An episode of silent MI discovered on ECG or Cardiac Imaging. Importantly = The mention of an MI on a report is enough to be considered as a prior MI and it is not necessary to retrieve the source document and/or documentation of this prior MI .

4. Patient affiliated to Social Security

5. Informed consent obtained in writing at enrolment into the study

Exclusion Criteria:

• Subjects presenting with any of the following will not be included in the study:

1. Uncontrolled arterial hypertension according to investigator decision

2. Prior episode of heart failure in the past two years of follow-up and/or low left ventricular ejection fraction <40% requiring the use of ßB;

3. New ACS (in the past 6 months) including UA/NSTEMI and STEMI;

4. Persistent angina or ischemia (>10% viable myocardium) requiring the use of ßB;

5. Prior episode of ventricular or supraventricular arrhythmia in the past year of follow-up requiring the use of ?B;

6. Treatment with other investigational agents or devices within the previous 30 days, or previous enrolment in this trial.

7. Pregnant Women or breast feeding women

8. Patient under legal protection (protection of the court, or in curatorship or guardianship).

Related Conditions & MeSH terms

• Infarction
• Myocardial Infarction

Intervention

Drug:
• Beta-blockers withdrawal
withdrawal of all type of betablockers
• Continuation of the Betablockers (ßB) treatment
Use Betablockers treatment

Locations

Country	Name	City	State
France	Institut de Cardiologie - USIC - Hôpital Pitié-Salpêtrière	Paris

Sponsors (2)

Lead Sponsor	Collaborator
Assistance Publique - Hôpitaux de Paris	Groupe Hospitalier Pitie-Salpetriere

Country where clinical trial is conducted

France, 

References & Publications (1)

Silvain J, Cayla G, Ferrari E, Range G, Puymirat E, Delarche N, Collet JP, Dumaine R, Slama M, Payot L, Kasty ME, Aacha K, Vicaut E, Montalescot G; ABYSS investigators of the ACTION Study Group,. betaeta blocker interruption after uncomplicated myocardial — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Anxiety and Depression	will be evaluated by using the HADS questionnaire to detect the presence of depression and anxiety ( there is no score; this will be determined by the response selected by the patient with "no" = no discomfort to "a lot" = significant discomfort	Through study completion, with a minimum of 1 year
Other	Erection Dysfunction	A precise evaluation of Erectile dysfunction will be proposed to male patients using an internationally validated questionnaire IIEF (International Index of Erectile Function) in French with 5 questions whose answer is graded from 0 to 5 per question	Through study completion, with a minimum of 1 year
Other	Libido	An evaluation of lack of sex drive will be evaluated by answering the following questions about the sexuality of the patient The frequency and degree of sex drive (self evaluation)	Through study completion, with a minimum of 1 year
Other	Exercise Capacity	will be evaluated by answering the following simple questions : The weekly physical activity and the sport practiced; Participation in competitions or not additionally, the recording the results of stress tests when available; Pre- and post - inclusion stress/ Strain test data	Through study completion, with a minimum of 1 year
Other	Side effects	will be evaluated by answering the following questions: Presence of Blury Vision, Sensation of cold hands and feets, Insomnia and palpitations	Through study completion, with a minimum of 1 year
Primary	The composite of Major Adverse Cardiovascular Events (MACE)	Will be evaluated with one-year minimum follow-up and will be the composite of Major Adverse Cardiovascular Events (MACE) including: All-cause death; Myocardial infarction (MI); Stroke; Hospitalisation for any cardiovascular (CV) reason.	Through study completion, with a minimum of 1 year
Secondary	Quality of life	will be evaluated by the questionnaire EQ5D-5L Score (0 to 1) and EQ5D-5L Scale (0 to 100) with higher scores indicating a better quality of Life.	Through study completion, with a minimum of 1 year