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Cardioprotection in CABG and AVR patients with RIPC

A two-centre randomised controlled trial investigating the effect of remote ischaemic preconditioning (RIPC) on blood and myocardial biomarkers of stress and injury-related signalling in patients having isolated coronary artery bypass grafting (CABG) or aortic valve replacement (AVR) using cardiopulmonary bypass (CPB)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN33084113
Enrollment
120
Registered
2013-03-25
Start date
2013-02-25
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Topic: Cardiovascular

Interventions

RIPC, Remote Ischaemic Pre-conditioning (RIPC) will be comprised of four 5 min cycles of right upper limb ischaemia, induced by a blood pressure cuff inflated to 200 mm Hg, with an intervening 5 min o

Sponsors

Imperial College London (UK)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 120 Years

Inclusion criteria

Inclusion criteria: Current inclusion criteria as of 03/11/2014: 1. Age =18 2. Patients undergoing elective (or urgent) first-time CABG or AVR Previous inclusion criteria: 1. Male and female, age >=40 and <85 years 2. Patients undergoing elective (or urgent) first-time CABG or AVR

Exclusion criteria

Exclusion criteria: Current exclusion criteria as of 03/11/2014: 1. Cardiogenic shock or cardiac arrest, 2. Significant peripheral arterial disease affecting upper limbs, 3. Renal failure (with a GFR 20 mmol/L, Prothrombin > 2.0 ratio) 4. Pulmonary disease (FEV1 < 40% predicted) 5. Renal failure (with a GFR < 30 ml/min/1.73m2) 6. Glibenclamide or nicorandil (as these medications may interfere with RIPC) 7. Participation in another interventional study

Design outcomes

Primary

MeasureTime frame
Myocardial Injury; Timepoint(s): 2 pre-operatively and 6, 12, 24, 48 and 72 hours after end of cardioplegic arrest

Secondary

MeasureTime frame
1. Clinical endpoints measured from admission up till 3 months post-operatively 2. Inflammatory and oxidative stress measured two pre-operatively and 5 postoperatively at 6, 12, 24, 48 & 72 hours after end of cardioplegic arrest

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 17, 2026