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Myocardial preconditioning in coronary artery bypass surgery

A clinical study investigating myocardial preconditioning in Type II diabetic patients in the setting of coronary artery bypass surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN01775128
Enrollment
500
Registered
2010-05-28
Start date
2006-02-20
Completion date
Unknown
Last updated
2017-05-08

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

Conditions

Topic: Cardiovascular

Interventions

The stimulus for RIPC that will be used will be inflation of a blood pressure cuff placed around the upper arm. The cuff will be inflated to 200 mmHg for 5 minutes after which it will be deflated for

Sponsors

University College London (UCL) (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged over 18 years 2. Patients undergoing coronary bypass surgery with or without concomitant heart valve surgeries 3. Male and female patients

Exclusion criteria

Exclusion criteria: 1. Aged under 18 years 2. Patients with severe renal impairment (estimated glomerular filtration rate less than 45 ml/min/1.73m2) 3. Patients with severe hepatic impairment 4. Patients with cardiac arrest in the previous 6 weeks

Design outcomes

Primary

MeasureTime frame
Myocardial injury, assessed by Troponin T and creatine kinase myocardial band (CK-MB) levels over the 72 hours post-CABG surgery.

Secondary

MeasureTime frame
1. Ionotropic score, measured at first week post-operative period 2. Ventilation times, measured at the timepoint when patients are weaned from ventilator in the ITU (first 2 days post-operative period) 3. Intensive care unit (ITU) stay, measured at first week post-operative period

Countries

United Kingdom

Outcome results

None listed

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