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Effect of Remote Ischemic Preconditioning on Cardiac Function After Cardiac Surgery

Effect of Remote Ischemic Preconditioning on Cardiac Function After Cardiac Surgery

Status
Withdrawn
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00882622
Enrollment
0
Registered
2009-04-16
Start date
2009-02-28
Completion date
2009-02-28
Last updated
2012-01-18

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

Conditions

Atrial Fibrillation, Cardiac Function, Myocardial Injury, Ventricular Arrythmias

Keywords

Ischemic Preconditioning, Cardiac Surgery

Brief summary

The purpose of this study is to evaluate the effects of Remote Ischemic Preconditioning on cardiac function in patients undergoing cardiac surgery compared to control intervention.

Detailed description

In detail, we will focus on new onset of atrial fibrillation, ventricular arrhythmias, myocardial injury, and cardiac function. Furthermore, we aim to investigate underlying pathways of RIPC in modifying the perioperative stress response.

Interventions

PROCEDURERemote Ischemic Preconditioning

RIPC will be induced during anesthesia by four 5-min cycles of upper limb ischemia and 5-min reperfusion using a blood-pressure cuff inflated to a pressure 15 mm Hg greater than the systolic arterial pressure measured via the arterial line.

PROCEDUREControl/sham procedure

Sham placement of the blood pressure cuff around the upper limb without inflation.

Sponsors

Goethe University
CollaboratorOTHER
Patrick Meybohm
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient undergoing heart surgery on cardiopulmonary bypass

Exclusion criteria

* Emergency cases * Myocardial infarction up to 7 days prior to enrollment * Ejection fraction less than 30% * Inability to give informed consent

Design outcomes

Primary

MeasureTime frame
New onset of atrial fibrillationWithin 30 days after surgery

Secondary

MeasureTime frame
Ventricular arrhythmias, myocardial injury, cardiac function. Underlying pathways of Remote Ischemic Preconditioning in modifying the perioperative stress response.Within 24 hours after surgery

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026