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Neuroprotection With Erythromycin in Cardiac Surgery

Perioperative Administration of Erythromycin and Brain Protection

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01274754
Enrollment
40
Registered
2011-01-12
Start date
2008-11-30
Completion date
2014-09-30
Last updated
2014-12-03

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

Conditions

Functional Disturbances Following Cardiac Surgery

Keywords

neuroprotection, erythromycin, neurocognitive assessment

Brief summary

Neurological complications occur in open heart surgery with a frequency of 40% and they range from major neurological deficits (due to a stroke) to neurocognitive and behavioral disorders. This study aims to determine if erythromycin, a worldwide known antibiotic, protects the brain from damage when given in high doses before and during open heart surgery. The investigators consume that high dose of erythromycin will protect the brain with a pharmacological preconditioning against the global ischemia during the perioperative period of heart surgery.

Detailed description

First Version: Study Protocol Authors: Thomaidou E., Vretzakis G., Argiriadou E., Stamatiou G., et al. Perioperative administration of erythromycin and brain protection Study Setting: On-pump, planned cardiac surgery. Randomized, double blinded clinical trial of two parallel groups. Group A: control group. Group B: erythromycin group (dose 25mg/kg intravenously). Purpose: Neurological complications occur in open heart surgery with a frequency of 40% and they range from major neurological deficits (due to a stroke) to neurocognitive and behavioral disorders. This study aims to determine if erythromycin, a worldwide known antibiotic, protects the brain from damage when given in high doses before and during open heart surgery. Hypothesis: The investigators consume that high dose of erythromycin will protect the brain with a pharmacological preconditioning against the global ischemia during the perioperative period of heart surgery. The aims of this study are: 1. To determine the effect of high-dose perioperative erythromycin administration on neurological outcome in patients undergoing cardiac surgery 2. To determine the relationship of neurological monitoring, specifically NIRS, to neurological outcomes and to determine if erythromycin affects this relationship. Preoperative Period Patient Exclusion Criteria: patients \> 80 years old, cerebrovascular disease with residual deficits, stroke, alcoholism, psychiatric disease. Preoperative patient neurocognitive status assessment from the same clinical psychologist in all patients: at least one day before surgery, perform neurocognitive tests. Patients of group A: 25mg/kg erythromycin intravenously 12 hours before surgery. Intraoperative Period Cerebral monitoring: continuous measurement and registration of cerebral oximetry data (NIRS - INVOS), record of frequency and duration of desaturation episodes (a fall \>20% compared to baseline values) and record of interventions to correct desaturation. Anaesthesia depth monitoring: continuous measurement of bispectral index (BIS). Registration of: duration of CPB and cross clamp time, mean arterial pressure, heart rate, temperature and ETCO2. Anesthesia Procedures: anesthesia induction with fentanyl 10-15μg/kg, propofol 2gm/kg and rocuronium 0,6mg/kg. Anesthesia maintenance with propofol. Postoperative Period - ICU Postoperative patient neurocognitive status assessment from the same clinical psychologist in all patients: On discharge, and 3 months later perform neurocognitive tests. Patients of group A: will receive high dose of erythromycin 12 hours after the end of surgery. Registration of: Post operative blood loss, duration of ICU stay, mechanical ventilation duration, duration of hospital stay, inotropic support, postoperative myocardial infarction, re-operation, dialysis, neurocognitive decline, other complications. BIOCHEMICAL INDEX Blood samples will be taken from all patients for the detection of tau protein, IL-1 and IL-6, 1. preoperatively 2. 12 hours after surgery 3. the 6th day after surgery

Interventions

None listed

Sponsors

University of Thessaly
CollaboratorOTHER
AHEPA University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* patients \< 80 years old scheduled for elective cardiac surgery coronary artery bypass grafting, good cooperation with the clinical psychologist

Exclusion criteria

* patients \> 80 years old * cerebrovascular disease with residual deficits * stroke * alcoholism * psychiatric disease

Design outcomes

Primary

MeasureTime frame
biochemical markers of brain ischemia and intraoperative cerebral oxymetry dataSeptember 2010

Secondary

MeasureTime frame
better neurocognitive outcome in Erythromycin groupNovember 2010

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026