Ischemic Heart DiseasePhase 4DAN-RELEASENCT07795398
DAN-RELEASE - Reconsidering Long-Term Aspirin in the Elderly Patients With Stable Ischemic Heart Disease
A Phase 4 study testing Continuation of daily low-dose Aspirin and Discontinuation of daily low-dose Aspirin in people with Ischemic Heart Disease and Ischemic Heart Disease Chronic, run by Odense University Hospital at 2 sites in Denmark.
Trial summary
DAN-RELEASE is a national, randomized, registry-based trial including 7,000 participants in Denmark. The trial aims to determine whether discontinuation of long-term aspirin therapy is non-inferior to continued aspirin therapy in older adults with stable ischemic heart disease. Read more about this study
- Who is it for?
- Ages 65 years and older
- Conditions the study is for
- Ischemic Heart Disease, Ischemic Heart Disease Chronic, Chronic Coronary Syndrome
- What is being tested?
- Continuation of daily low-dose Aspirin and Discontinuation of daily low-dose Aspirin
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 7,000 participants
- Where
- 2 sitesDenmark
- Study dates
- 30 Sep 2026to Oct 2029
- Phase
- Phase 4
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 65 years and older
- All sexes
- No healthy volunteers
- Older adult
Who may be able to join
- Age ≥65 years at randomization
- Ischemic heart disease (IHD) with index event (myocardial infarction (MI), percutaneous coronary intervention (PCI), or coronary artery bypass grafting (CABG)) >2 years previously
- Since index event free from ischemic cardiovascular events (MI, ischemic stroke, or transitory ischemic attack) or any coronary revascularization procedure (PCI/CABG)
- Currently treated with low dose aspirin (≤150 mg daily)
Who cannot join
- History of ischemic stroke
- Active treatment with or indication for anti-coagulant or P2Y12-inhibitor therapy
- Indication for antiplatelet treatment other than secondary prevention of IHD according to treating physician (i.e. haematological diseases, peripheral artery disease)
- Any revascularization procedure for peripheral artery disease
- Any history of stent thrombosis or stenting of the left main coronary artery
- Other contraindications to aspirin discontinuation according to treating physician
- Not being able to understand Danish
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Denmark2 sites, 2 recruiting
- Recruiting
Bispebjerg Frederiksberg Hospital
Copenhagen
Eva Prescott, Prefessor, MD, MDSc, Eva.Irene.Bossano.Prescott@regionh.dk
- Recruiting
Odense Universitetshospital
Odense, 5000
Axel Diederichsen, MD, PhD, +4540191227, axel.diederichsen@rsyd.dk
About this study
Official title: The RELEASE Trial: Reconsidering Long-Term Aspirin in the Elderly in Secondary Prevention of Cardiovascular Disease
DAN-RELEASE is a national, randomized, registry-based trial including 7,000 participants in Denmark. The trial aims to determine whether discontinuation of long-term aspirin therapy is non-inferior to continued aspirin therapy in older adults with stable ischemic heart disease.
Long-term aspirin therapy is recommended for patients with established ischemic heart disease. However, among clinically stable patients years after percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG), or myocardial infarction (MI), the evidence supporting lifelong aspirin therapy is limited. At the same time, the risk of serious bleeding increases with age.
DAN-RELEASE will therefore compare aspirin discontinuation with continued aspirin therapy in adults aged 65 years or older with stable ischemic heart disease who have remained free from ischemic events for at least two years. The trial will assess whether discontinuing aspirin is non-inferior to continued treatment with respect to cardiovascular and bleeding outcomes.
Read the detailed description
Rationale:
Current guidelines recommend life-long aspirin therapy in patients with chronic coronary syndrome. The evidence supporting long-term aspirin therapy after myocardial infarction (MI) and for chronic coronary syndrome stems primarily from trials conducted in the 1970s and 1980s. Since then, the clinical landscape of MI has evolved markedly: The use of highly sensitive cardiac troponins has led to the diagnosis of smaller MIs, coinciding with a shift from predominantly large ST-segment elevation MI (STEMI) to smaller non-STEMI. Acute revascularization is now a part of the routine care for MI and many patients with stable coronary artery disease undergo percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG). Population risk factors have improved, and universal use of statins have contributed to plaque stabilization and reduces progression of disease. As a result, long-term prognosis in patients with MI and chronic coronary syndromes has markedly improved.
Therefore, the absolute ischemic benefit of long-term aspirin therapy may be attenuated, while the risk of bleeding, particularly in older patients, remains clinically relevant. These developments warrant a contemporary re-evaluation of the life-long role of aspirin in long-term secondary prevention of cardiovascular disease, especially in elderly patients with stable disease.
Objective:
To evaluate whether discontinuation of long-term aspirin in elderly patients with stable chronic coronary syndrome is non-inferior to continued aspirin therapy with respect to net clinical outcome.
All clinical outcomes will be registry based except patient-reported outcomes. They will be assessed using questionnaires measuring bleeding symptoms, gastrointestinal discomfort, quality of life and lifestyle behaviour during follow-up.
Trial design:
Investigator-initiated, registry-based, prospective, randomized, open-label, blinded endpoint (PROBE) non-inferiority trial with 1:1 allocation. The trial is conducted as a low-intervention clinical trial using nationwide Danish health registries as the primary data source.
Risk-benefit considerations:
Aspirin is widely used in secondary prevention and is available over the counter, reflecting its well established safety profile and the generally low risk associated with its use. Nevertheless, aspirin is associated with potential adverse effects, including bleeding, gastrointestinal discomfort, and clinically relevant drug interactions, particularly in elderly patients with comorbidities. Based on data from national health registries, the target population - older adults with stable chronic coronary syndrome - represents a clinically stable group with a low event rate of ischemic events. Given that lifelong aspirin therapy is often continued without systematic reassessment, there is a clear ethical justification for evaluating whether continuation remains beneficial - and safe - in an aging population with changing comorbidity profiles.
- Conditions
- Ischemic Heart Disease, Ischemic Heart Disease Chronic, Chronic Coronary Syndrome, Myocardial Infarction, Percutaneous Coronary Intervention, Coronary Artery Bypass Graft
- Being tested
- Continuation of daily low-dose Aspirin, Discontinuation of daily low-dose Aspirin
- Keywords
- Ischemic heart disease, Chronic coronary syndrome
- Medical subject headings
- Myocardial Ischemia, Myocardial Infarction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Continuation of daily low-dose AspirinDrug
Also called continuation of Aspirin
Participants randomized to this intervention will continue their current daily low-dose aspirin therapy.
Discontinuation of daily low-dose AspirinDrug
Also called Discontinuation of Aspirin
Participants randomized to this intervention will discontinue their current daily low-dose aspirin therapy.
| Study group | Role | What they receive |
|---|---|---|
| Continuation of Aspirin | Active comparator | Participants randomized to this arm will continue their current long-term low-dose aspirin therapy. Receives: Drug: Continuation of daily low-dose Aspirin |
| Discontinuation of Aspirin | Active comparator | Participants randomized to this arm will discontinue their current long-term low-dose aspirin therapy. Receives: Drug: Discontinuation of daily low-dose Aspirin |
What is being measured
The primary outcome is the main question the study is designed to answer.
Hierarchical Composite of Cardiovascular and Bleeding Events
A hierarchical composite endpoint using a win-ratio framework combining cardiovascular death, fatal bleeding, intracranial bleeding, Myocardial infarction, ischemic stroke, and bleeding events (BARC 3-5).
Measured: From randomization until the end of the study, with a minimum follow-up of 1 year
Secondary outcomes (13)
Cardiovascular Death
Death due to a cardiovascular cause.
Measured: From randomization until the end of the study, with a minimum follow-up of 1 year
Fatal Bleeding (BARC Type 5)
Fatal bleeding classified as Bleeding Academic Research Consortium (BARC) type 5.
Measured: From randomization until the end of the study, with a minimum follow-up of 1 year
Intracranial Bleeding (BARC Type 3c)
Intracranial bleeding classified as Bleeding Academic Research Consortium (BARC) type 3c.
Measured: From randomization until the end of the study, with a minimum follow-up of 1 year
Ischemic Stroke
Occurrence of ischemic stroke during follow-up.
Measured: From randomization until the end of the study, with a minimum follow-up of 1 year
Myocardial Infarction
Occurrence of myocardial infarction during follow-up.
Measured: From randomization until the end of the study, with a minimum follow-up of 1 year
Other Major Bleeding (BARC Types 3a and 3b)
Major bleeding classified as Bleeding Academic Research Consortium (BARC) types 3a or 3b.
Measured: From randomization until the end of the study, with a minimum follow-up of 1 year
All-Cause Mortality
Death from any cause during follow-up.
Measured: From randomization until the end of the study, with a minimum follow-up of 1 year
Hospitalization for Cardiovascular Causes
Hospitalization due to cardiovascular causes during follow-up.
Measured: From randomization until the end of the study, with a minimum follow-up of 1 year
Peptic Ulcer
Occurrence of peptic ulcer during follow-up.
Measured: From randomization until the end of the study, with a minimum follow-up of 1 year
Minor Bleeding
Patient-reported bleeding symptoms will be assessed using a modified version of the International Society on Thrombosis and Haemostasis Scientific and Standardization Committee Bleeding Assessment Tool (ISTH/SSC-BAT). The questionnaire is used to collect information on bleeding symptoms not available from national health registries.
Measured: From randomization until the end of the study, with a minimum follow-up of 1 year
Abdominal Pain and Discomfort
Patient-reported abdominal pain and gastrointestinal discomfort during follow-up, including symptom burden and impact on daily life. Individual questionnaire items are assessed separately, and no overall scale score is calculated.
Measured: Baseline and 3, 6, 12, and 24 months after randomization
Quality of Life (EQ-5D-5L)
Patient-reported health-related quality of life assessed using the EQ-5D-5L (EuroQol 5-Dimension 5-Level) questionnaire.
The descriptive system covers five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension is rated on five levels, ranging from no problems (level 1) to extreme problems or inability (level 5), with higher levels indicating worse health status. The responses to the five dimensions are combined into a five-digit health state.
The direct sum of the 5 individual dimension scores. Higher means worse health status. The EQ Visual Analogue Scale (EQ VAS) records the participant's self-rated health on a scale from 0 to 100, where 0 represents the worst health imaginable and 100 represents the best health imaginable. Higher EQ VAS scores indicate better self-rated health.
Measured: Baseline and 3, 6, 12, and 24 months after randomization
Angina Symptoms, Frequency, and Physical Limitations (Seattle Angina Questionnaire)
Patient-reported angina symptoms, frequency, and physical limitations assessed using the 7-item Seattle Angina Questionnaire (SAQ-7). Scores are transformed to a scale from 0 to 100, with higher scores indicating better health status and fewer limitations due to angina.
Measured: Baseline and 3, 6, 12, and 24 months after randomization
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted31 Aug 2026
- Study start30 Sep 2026
- Primary completionOct 2029 (estimated)
- Study completionOct 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Ischemic Heart DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Participants are randomized 1:1 to continuation or discontinuation of low-dose aspirin.
- Masking
- None (open label)
- Enrolment
- 7,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Odense University Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- University Hospital Bispebjerg and Frederiksberg
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07795398
- Sponsor's protocol ID
- 2026-525442-30
- Other IDs
- 2026-525442-30-00
- Acronym
- DAN-RELEASE
- Status last verified
- Oct 2026
- First submitted
- 26 Aug 2026
- Last updated
- 5 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Due to data protection requirements, individual participant data are not planned to be shared outside the study research group.