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Elucidating the mechanistic pathways of ischaemic preconditioning and postconditioning in the clinical setting

A multicentre randomised interventional treatment trial to explore the mechanistic pathway of ischaemic preconditioning and postconditioning in the clinical settings of myocardial ischaemia-reperfusion injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN49989273
Enrollment
400
Registered
2010-06-18
Start date
2007-06-01
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

Topic: Cardiovascular

Interventions

1. Intervention 1: Cyclosporin A at dose of 2.5 mg/kg
diluted in 100 ml of normal saline. Once only dose given over 30 minutes prior to surgery. 2. Intervention 2: Atorvastatin at a dose of 160 mg
given on the morning of surgery and a second dose of 160 mg repeated 24 hours later 3. Intervention 3: Erythropoietin at a dose of 50,000 IU
given as an infusion of 50 ml over 30 minutes prior to revascularisation. A second dose is repeated 24 hours later.

Sponsors

University College London (UCL) (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients experiencing an event or procedure which will bring about myocardial injury: 1. Coronary artery bypass surgery +/- valve surgery 2. Primary angioplasty for ST elevation myocardial infarction 3. Thrombolysis for ST elevation myocardial infarction 4. Non-ST elevation myocardial infarction 5. High risk and undergoing percutaneous coronary intervention 6. Aged 18 - 85 years, either sex

Exclusion criteria

Exclusion criteria: 1. Significant co-morbidity 2. Known intolerance to trialled intervention 3. Renal/liver failure 4. In patients undergoing an elective procedure-chest pain within the last 3 days, lack of consent

Design outcomes

Primary

MeasureTime frame
Serum cTnT and CK-MB (bloods taken before intervention and at 6, 12, 24, 48 and 72 hours post-intervention).

Secondary

MeasureTime frame
1. Inotropic score: calculated using the maximum inotropic dose used on day 1 post-op 2. Ventilation time: assessed from the time of admission into ITU to the time of extubation 3. ITU stay: assessed from the time of admission into ITU to the time of discharge from the unit

Countries

United Kingdom

Outcome results

None listed

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