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The incidence of cardiac arrhythmia in coronary artery bypass surgery

comparison the effectiveness of dexmedetomidine with midazolam on incidence of cardiac arrhythmia in off-pump coronary artery bypass surgery patients, a clinical trial.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016072413159N9
Enrollment
40
Registered
2016-07-30
Start date
2016-08-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Cardiopulmonary bypass. Pulmonary heart disease, unspecified

Interventions

Intervention 1: Control group: Patients are receiving 0.5 mg/kg midazolam addition of 10 mcg/kg fentanyl, 0.5 mg/kg atracurium, and 1.5 mg/kg propofol for induction of anesthesia. Cardiac arrhythmia r
Treatment - Drugs
Control group: Patients are receiving 0.5 mg/kg midazolam addition of 10 mcg/kg fentanyl, 0.5 mg/kg atracurium, and 1.5 mg/kg propofol for induction of anesthesia. Cardiac arrhythmia rate and hemodyna
Interventional group: Patients are receiving 1 mcg/kg dexmedetomidine infusion for induction of anesthesia for 10 minutes, and then infusion is fallowing up with 0.2 to 0.6 mg/kg/h based on tolerance

Sponsors

Vice Chancellor for Research, Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients undergoing off-pump coronary artery bypass surgery; sustaining ASA I and ASA II; aged between 18-75 years; EF more than 35%. Exclusion criteria: History of arrhythmias or heart block; EF less than 35%; history of cardiac surgery; history of valvular heart disease; having left atrial enlargement (LAE) or cardiomegaly.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Cardiac arrhythmia rate. Timepoint: During and 24 hours after surgery. Method of measurement: Heart monitoring.

Secondary

MeasureTime frame
Hemodynamic changes. Timepoint: During and 24 hours after surgery. Method of measurement: Heart monitoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShima Shebani

Mashhad University of Medical Sciences

sheybanish@mums.ac.ir+98 51 3801 2612

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 8, 2026