Skip to main content
OpenTrials
Completed

NCT Number: NCT02554006

Predischarge Bundle to Minimize Negative Impact on Quality of Life of Nuisance Bleedings

A single-center, randomized trial of admitted patients with ischemic heart disease receiving percutaneous coronary intervention and stent implantation will be conducted at University Hospital of Ferrara. Patients will be randomized to either the control (standard care) or the bundle group in which patients will receive counseling regarding dual antiplatelet therapy management, advantages and side effects, screening for depression or anxiety, standardized education. The primary endpoint will be the difference in the quality of life as assessed by EQ-5D questionnaire.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital of Ferrara

Cona, Ferrara, 44124, Italy

About this study

Recent studies suggest that bleeding complications have a strong influence on quality of life. During DAPT regimen bleeding complications occur from 5% to 15% of patients. Nuisance bleedings (BARC 1 bleeding) occur more frequently and show a strong influence on quality of life, depression, anxiety and compliance to the treatment.

The aim of the study is to establish if a specific counseling programme might minimize the negative quality of life impact of nuisance bleedings. A computer-generated list will be used to randomize patients in a 1:1 ratio, stratified by age, sex, renal failure and P2Y12 inhibitor, to either the bundle or the control group.

All patients randomized to the control group (standard of care) will receive education from physician regarding dual antiplatelet therapy (DAPT) as part of the routine discharge process.

All patients randomized to the bundle group will receive:

i) a 15-min visit by a member of the research team 24 h prior to the anticipated discharge day. During this visit, a core set of DAPT risks will be addressed. Advantages and side effects of DAPT will be described. The importance of compliance will be discussed. The correct management of side effects (especially BARC 1 bleedings) will be discussed.

ii) a 15-min visit by a member of the research team with a family member living near/with the patient. Advantages and side effects of DAPT will be described. The importance of compliance will be discussed. The correct management of side effects (especially BARC 1 bleedings) will be discussed.

iii) brochure describing advantages, side effects and management of dual antiplatelet therapy. Contemporaneously, the investigators of the study will contact directly by phone and/or mail the general practionnaire of the patient to describe and explain the same topics and the clinical problem of her patient.

iv) availability of phone number to discuss potential side effects of DAPT. In addition, the study coordinator of the study will contact two times by month the patient by phone to assess DAPT compliance and potential BARC 1 bleedings.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • signed written informed consent
  • hospital admission for ischemic heart disease with clinical indication to coronary artery angiography
  • percutaneous coronary intervention and drug eluting stent implantation
  • indication to dual antiplatelet therapy for at least 6 months

Exclusion criteria

  • oral anticoagulant therapy
  • bleeding event in the 30 days before the enrolment
  • planned surgery

Treatment and study plan

good clinical practice

Behavioral

education from physician regarding dual antiplatelet therapy as part of the routine discharge process

Other names: standard of care

bundle group

Behavioral

visits and materials describing advantages and side effects of dual antiplatelet therapy and their management

Other names: counseling regarding dual antiplatelet therapy management

Primary outcomes

  1. quality of life

    Time frame: 1 month

    quality of life assessment in each patient by EQ-5D questionnaire

Secondary outcomes

  1. emergency room admission

    Time frame: 1 month

    number of access to emergency room service for bleeding

  2. general practitioner visit

    Time frame: 1 month

    number of access to general practitioner for bleeding

  3. dyspnea occurrence

    Time frame: 1 month

    number of patients suffering dyspnoea stratified according P2Y12 inhibitors

  4. bleeding academic research consortium (BARC) 2-3

    Time frame: 1 month

    occurrence of BARC 2-3 complications

  5. bleeding academic research consortium (BARC) 1

    Time frame: 1 month

    occurrence of BARC 1 complications

Other outcomes

  1. ischemic adverse events

    Time frame: 1 year

    cumulative incidence of the following ischemic adverse events: cardiac death, myocardial infarction, transient ischemic attack/stroke

  2. all-cause mortality

    Time frame: 1 year

    occurrence of all-cause death

  3. BARC 1-3

    Time frame: 1 year

    occurrence of BARC1-3 complications

Sponsors and collaborators

Lead sponsor

University Hospital of Ferrara

Other

Registry information

Official study title

Predischarge Bundle for Patients in Dual Antiplatelet Therapy to Minimize the Negative Impact of Nuisance Bleedings on Quality of Life: a Randomized Controlled Trial.

Acronym: BATMAN

Important dates

Study start
2015
Primary completion
2016
Study completion
2017
First posted
Sep 18, 2015
Registry last updated
May 2, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.