Systematic Screening for Risk-factors for Ulcer Bleeding Before Anti-thrombotic Treatment
Primary Purpose
Coronary Occlusion/Thrombosis, Peptic Ulcer Hemorrhage
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Screening for risk factors for ulcer bleeding
Sponsored by
About this trial
This is an interventional screening trial for Coronary Occlusion/Thrombosis
Eligibility Criteria
Inclusion Criteria:
- Patients who has had a PCI with stenting or balloon dilatation in the cardiology department at Odense University Hospital, Århus University Hospital and Ålborg Sygehus, where subsequent treatment with low-dose aspiring and clopidogrel or another thienopyridine is planned for one year.
Exclusion Criteria:
- previous PCI with stenting or balloon dilatation
- treatment with clopidogrel prior to PCI
- lack of informed consent
Sites / Locations
- Odense University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Active Comparator
Arm Label
Control group
Screening and risk assessment
Arm Description
Outcomes
Primary Outcome Measures
Admission for ulcer bleeding or haemorrhagic gastritis
Efficacy of a systematic screening for risk factors for ulcer bleeding in patients, who after percutaneous coronary intervention (PCI), is treated with antithrombotic medicine
Secondary Outcome Measures
Compliance with antithrombotic medicine
Does prophylactic treatment with proton pump inhibitor increase the compliance with antithrombotic medicine and thereby decrease the risk of new cardiac event.
Identification of patients with benefit of proton pump inhibitor prophylaxis
Analysis of risk factors is planned in order to define which patients have the greatest benefit of PPI prophylaxis when receiving antithrombotic treatment.
Gastrointestinal bleeding
Admission to hospital for not endoscopic verified upper gastrointestinal bleeding.
Uncomplicated ulcers
Development of uncomplicated ulcers
Death
Registration of cause of death
Acute coronary syndrome
Re-admission for acute coronary syndrome, including stent occlusion
Full Information
NCT ID
NCT01447498
First Posted
September 26, 2011
Last Updated
November 9, 2015
Sponsor
Odense University Hospital
Collaborators
Aarhus University Hospital, Danish Heart Foundation, Region of Southern Denmark
1. Study Identification
Unique Protocol Identification Number
NCT01447498
Brief Title
Systematic Screening for Risk-factors for Ulcer Bleeding Before Anti-thrombotic Treatment
Official Title
Effect of a Systematic Screening for Risk-factors for Ulcer Bleeding Before Post-PCI Anti-thrombotic Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Odense University Hospital
Collaborators
Aarhus University Hospital, Danish Heart Foundation, Region of Southern Denmark
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
In a prospective randomised study design to investigate, if a systematic risk factor screening for bleeding ulcer in patients, who following percutaneous coronary intervention (PCI) commence a one year combination treatment with low dose aspirin and clopidogrel, followed by prophylactic treatment with a proton pump inhibitor (PPI) in case of increased risk, can reduce the risk of bleeding ulcer. Based on the recently raised suspicion that PPI's, possibly except pantoprazole, reduce the effect of ADP-receptor inhibitors, pantoprazole has been chosen as prophylaxis in the screening group, and analyses will be done to ascertain whether PPI treatment increases the risk of coronary events. Further analyses will be made to see whether PPI prophylaxis in high risk patients can increase compliance with the antithrombotic treatment through a reduction of side effects, thereby reducing the risk of myocardial infarction in particular stent thrombosis. The study population will be analyzed further to identify the patients, who will benefit the most from PPI prophylaxis Hypothesis: screening heart patients for risk factors for bleeding ulcer and subsequently treating high risk patients with PPI can reduce the incidence of bleeding ulcer and increase compliance with the antithrombotic treatment; thereby possibly reducing the risk of coronary events and improving survival. Initial a description of the prevalence of risk factors will be done.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Occlusion/Thrombosis, Peptic Ulcer Hemorrhage
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2024 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control group
Arm Type
No Intervention
Arm Title
Screening and risk assessment
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Screening for risk factors for ulcer bleeding
Intervention Description
Following PCI the patients fill out a questionnaire to assess the risk factors for ulcer bleeding.We randomise between:
screening and risk assessment
control group
All screened patients, who fulfil the criteria for having a moderate to high risk of ulcer bleeding will be sent written information about risk factors and the purpose of the PPI prophylaxis. They will be recommended PPI prophylaxis (Pantoprazole), as long as they are being treated with low-dose aspirin and clopidogrel.
Patients in the screening group, who are already on PPI treatment is recommended to change to Pantoprazole.
Definition of risk of ulcer bleeding: The table below will be used for screening. Patients scoring ≥ 2 points will receive PPI prophylaxis.
points: Age: < 60: 0; 60-69: 1; 70-79: 2; >=80: 3 ___ Dyspepsia: 1 ___ Uncomplicated ulcer: 2 ___ Complicated ulcer 3 ___ NSAID 2 ___ Steroids 2 ___ SSRI 2 ___ Anticoagulant Tx 2 ___
Primary Outcome Measure Information:
Title
Admission for ulcer bleeding or haemorrhagic gastritis
Description
Efficacy of a systematic screening for risk factors for ulcer bleeding in patients, who after percutaneous coronary intervention (PCI), is treated with antithrombotic medicine
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Compliance with antithrombotic medicine
Description
Does prophylactic treatment with proton pump inhibitor increase the compliance with antithrombotic medicine and thereby decrease the risk of new cardiac event.
Time Frame
1 year
Title
Identification of patients with benefit of proton pump inhibitor prophylaxis
Description
Analysis of risk factors is planned in order to define which patients have the greatest benefit of PPI prophylaxis when receiving antithrombotic treatment.
Time Frame
1 year
Title
Gastrointestinal bleeding
Description
Admission to hospital for not endoscopic verified upper gastrointestinal bleeding.
Time Frame
1 Year
Title
Uncomplicated ulcers
Description
Development of uncomplicated ulcers
Time Frame
1 year
Title
Death
Description
Registration of cause of death
Time Frame
1 Year
Title
Acute coronary syndrome
Description
Re-admission for acute coronary syndrome, including stent occlusion
Time Frame
1 Year
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients who has had a PCI with stenting or balloon dilatation in the cardiology department at Odense University Hospital, Århus University Hospital and Ålborg Sygehus, where subsequent treatment with low-dose aspiring and clopidogrel or another thienopyridine is planned for one year.
Exclusion Criteria:
previous PCI with stenting or balloon dilatation
treatment with clopidogrel prior to PCI
lack of informed consent
Facility Information:
Facility Name
Odense University Hospital
City
Odense
ZIP/Postal Code
5000
Country
Denmark
12. IPD Sharing Statement
Learn more about this trial
Systematic Screening for Risk-factors for Ulcer Bleeding Before Anti-thrombotic Treatment
We'll reach out to this number within 24 hrs