Computer tool helps doctors choose better heart meds after attack
NCT ID NCT05844566
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a computer-based decision support system (DSS) helps doctors start or intensify cholesterol-lowering treatments earlier in patients who have had a heart attack. Over 1,100 patients from multiple hospitals took part. The DSS provided risk estimates but did not recommend specific drugs. Researchers compared outcomes between hospitals using the DSS and those providing standard care alone.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Decision Support System (DSS) - a computer tool that shows risk estimates
- What this could lead to
- If successful, this tool could help doctors make quicker, more effective decisions about cholesterol-lowering treatments after a heart attack, potentially reducing future heart risks.
- What could go wrong
- This is a completed trial, but the tool only provides information—it doesn't guarantee better outcomes. Results may not apply to all hospitals or patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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1,139 people
The number who actually took part.
- Started
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Apr 2023
- Finished
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Dec 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 79 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: Sites: * Manage ACS patients as defined by: Symptoms of myocardial ischemia with an unstable pattern, occurring at rest or with minimal exertion, within 72 hours of an unscheduled hospital admission due to presumed or proven obstructive coronary disease and at least one of the following: * Elevated cardiac biomarkers * Resting electrocardiographic changes consistent with ischemia or infarction, plus additional evidence of obstructive coronary disease from regional wall motion or perfusion abnormality, 70% or more epicardial coronary stenosis by angiography, or need for coronary revascularization procedure * Mange post ACS follow up care of patients including risk factor control * Ability to provide follow up information on patient care for a minimum of 16 weeks including blood tests * Willing/ able to access and undertake training for the DSS * Adequate internet connection at site and the ability to access the DSS * No restrictions on use of LLTs (within national guidelines/ reimbursement) * Ability to include all essential parameters and patient information for DSS input Participants: * Aged ≥18 to \< 80 years old * Provide written informed consent * Presenting to a study site with ACS as LLT naïve, monotherapy or combination therapy (defined as more than one LLT agent) * Willing to take lipid lowering treatments for the secondary prevention of cardiovascular disease * Attending the same study site (or same clinical team) for ACS follow up to ensure follow up data can be collected; or ensure that follow up data can be collected from other clinical institutions as part of the clinical pathway. Exclusion criteria: Sites: * Unable to capture/ provide data on patients with ACS during admission and follow up * Unable or unwilling to use lipid lowering treatments other than statins for ACS care Participants: * Unable to provide written informed consent * LDL-C measurement \< 1.8 mmol/L at admission
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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A.O.U Policlinico di Modena S.C. di Cardiologia
Modena, 41124, Italy
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A.O.U. Ospedali Riuniti U.O.C. Cardiologia e UTIC
Foggia, 71122, Italy
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AUSL di Bologna-Ospedale Maggiore
Bologna, 40133, Italy
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AUSL-IRCCS di Reggio Emilia
Reggio Emilia, 42121, Italy
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Azienda Ospedaliera Universitaria Gaetano Martino
Messina, 98125, Italy
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Azienda Ospedaliera di Rilievo Nazionale (A.O.R.N.) "Sant'Anna e San Sebastiano" di Caserta
Caserta, 81100, Italy
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Azienda Ospedaliero Universitaria Santa Maria della Misericordia
Udine, 33100, Italy
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Calderdale Royal Hospital
Halifax, West Yorkshire, HX3 0PW, United Kingdom
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Conquest Hospital
Brighton, East Sussex, TN37 7PT, United Kingdom
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Freeman Hospital
Newcastle upon Tyne, Tyne and Wear, NE7 7DN, United Kingdom
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Glan Glwyd Hospital
Bodelwyddan, Denbighshire, LL18 5UJ, United Kingdom
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Gregorio Marañón General University Hospital
Madrid, 28007, Spain
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Hammersmith Hospital
London, W2 1NY, United Kingdom
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Hospital Clínico Universitario Santiago de Compostela
Santiago de Compostela, A Coruña, 15706, Spain
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Hospital Clínico Universitario Virgen de la Arrixaca
El Palmar, Murcia, 30120, Spain
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Hospital HM Montepríncipe
Boadilla del Monte, Madrid, 28660, Spain
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Hospital Universitario Fundación Jiménez Díaz
Madrid, 28040, Spain
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Hospital Universitario La Luz Quiron
Madrid, 28003, Spain
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Hospital Universitario La Paz
Madrid, 28046, Spain
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Hospital Universitario Reina Sofia
Córdoba, 14004, Spain
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Hospital Universitario Rey Juan Carlos
Móstoles, Madrid, 28933, Spain
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Hospital Universitario Virgen Macarena
Seville, 41009, Spain
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Hospital de la Santa Creu i Sant Pau
Barcelona, 08025, Spain
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IRCCS Policlinico San Donato
Milan, 20097, Italy
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IRCCS. A.O.U. Policlinico San Martino IST
Genova, 16132, Italy
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Kettering General Hospital
Kettering, Northamptonshire, NN16 8UZ, United Kingdom
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Luton and Dunstable University Hospital
Luton, Bedfordshire, LU4 0DZ, United Kingdom
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North Tyneside General Hospital
North Shields, Tyne and Wear, NE29 8NH, United Kingdom
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Ospedale Sandro Pertini - ASL Roma 2
Roma, 00157, Italy
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Ospedale di Cisanello - A.U.O.P. Azienda Ospedaliera Universitaria
Pisa, 56124, Italy
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Puerta de Hierro Majadahonda University Hospital
Madrid, 28222, Spain
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Royal Bournemouth Hospital
Bournemouth, Dorset, BH7 7DW, United Kingdom
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Royal United Hospital
Bath, Somerset, BA1 3NG, United Kingdom
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Russell's Hall Hospital
Dudley, West Midlands, DY12HQ, United Kingdom
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Sandwell General Hospital
Birmingham, West Midlands, B71 4HJ, United Kingdom
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Scunthorpe General Hospital
Scunthorpe, North Lincolnshire, DN15 7BH, United Kingdom
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Southern Health and Social Care Trust, Craigavon Area Hospital
Portadown, Northen Ireland, BT63 5QQ, United Kingdom
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Sunderland Royal Hospital
Sunderland, Tyne and Wear, SR4 7TP, United Kingdom
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University Hospital of A Coruña
A Coruña, Coruña, 15006, Spain
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Vall d'Hebron University Hospital
Barcelona, 08035, Spain
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Worcestershire Royal Hospital
Worcester, Worcestershire, WR5 1DD, United Kingdom
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Worthing Hospital
Worthing, West Sussex, BN11 2DH, United Kingdom
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a 20-Minute playlist calm a heart attack Patient's nerves?
- A blood test at 50 could flag your risk of five diseases. can an app stop them?
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- Broken heart syndrome: is it as deadly as a heart attack?
- Fat graft may mend heart scars after a heart attack