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Impact of comprehensive and intensive treatment of risk factors concerning cardiovascular mortality in secondary prevention: MIRVAS study

Impact of comprehensive and intensive treatment of risk factors concerning cardiovascular mortality in secondary prevention: MIRVAS study - a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN93700442
Enrollment
247
Registered
2009-02-19
Start date
2002-09-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Secondary prevention of cardiovascular disease Circulatory System

Interventions

The MIRVAS study is a randomised controlled trial conducted at La Princesa University Hospital. Patients were included in the study between September 2002 and February 2004. On the day of admission

Sponsors

La Princesa University Hospital (Hospital Universitario de La Princesa) (Spain)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Both males and females, from 18 to 80 years old 2. Patients admitted to the hospital for acute coronary syndrome (with or without ST-segment elevation) or an ischaemic stroke

Exclusion criteria

Exclusion criteria: 1. Refusal or inability to participate in the follow-up (displaced patients or with reduced mobility) 2. Life expectancy of less than 12 months 3. Severe cognitive deterioration

Design outcomes

Primary

MeasureTime frame
The following were assessed at three-year follow-up: 1. Cardiovascular mortality and cardiovascular morbimortality, which included the following events: 1.1. Cardiovascular death 1.2. Acute coronary syndrome with or without ST-segment elevation 1.3. Acute stroke (ischaemic or haemorrhagic) 1.4. Revascularisation in any area 1.5. Amputation as a result of peripheral ischaemia 2. Admittance due to heart failure 3. Control of risk factors All episodes were understood as such if they had a clinical report to back them up. The assessments were carried out by an unblinded member of the research group.

Secondary

MeasureTime frame
The following were assessed at 1 and 3 years: 1. Percentage of patients who reached the optimal control of each risk factor 2. Percentage of pharmacological interventions recommended by international guidelines for secondary prevention of cardiovascular risk received in each arm

Countries

Spain

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026