A comparative study on the postoperative recovery between balanced and total intravenous anesthesia in patients undergoing off-pump coronary artery bypass surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0004726

Enrollment

102

Registered

2020-02-11

Start date

2020-02-19

Completion date

Unknown

Last updated

2022-11-28

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

Conditions

None listed

Interventions

Drug : Patients randomized to the Balanced anesthesia group induce anesthesia by propofol (1–1.5 mg/kg) or etomidate (0.2–0.5 mg/kg) to achieve bispectral index (BIS) of 40–60. Sufentanil loading dose

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who are American sociaty of anesthesiologist physical status I, II, III, IV Patients aged 20–80 year Patients Undergoing Coronary Artery Bypass Surgery under general anesthesia Patients who have voluntarily agreed to participate in this study

Exclusion criteria

Exclusion criteria: Patients who have taken sleeping pills, antipsychotics or narcotic analgesics for more than 1 week Patient who had mental retardation Patient with iliteracy Conversion to on-pump coronary artery bypass surgery Patients with left ventricular ejection fraction less than 30% Major organ failure before surgery (plasma creatine more than 2 mg/dL, AST / ALT with greater than three times normal elevations, with persistent elevations, neurological abnormalities) Patients who continue to need mechanical ventilation after surgery

Design outcomes

Primary

Measure	Time frame
Quality of recovery-40 (QoR-40)	—

Secondary

Measure	Time frame
heart rate;blood pressure	—

Countries

Korea, Republic of

Contacts

Public ContactJoungmin Kim

Chonnam National University Hospital

tca77@hanmail.net+82-62-220-6895

Outcome results