Registry for Perioperative Data in Patients Undergoing Cardiac Surgery

Completed

• Conditions: Anesthesia; Cardiac Surgical Procedures

• Registration Number: NCT01713192
• Lead Sponsor: Seoul National University Hospital

Brief Summary

The purpose of this registry is to obtain perioperative data in patients undergoing cardiac surgery and find out relations between the data and investigate several causes affecting postoperative complications.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2012-10-22
• Study First Submitted QC: 2012-10-23
• Study First Posted: 2012-10-24
• Study Start: 2013-01
• Primary Completion: 2014-09
• Study Completion: 2014-09
• Status Verified: 2015-11
• Last Update Submitted: 2015-11-16
• Last Update Posted: 2015-11-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

• patients undergoing cardiac surgery

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Exclusion Criteria

• refused to participate

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
perioperative data	1 year after surgery	To obtain the perioperative data in patients undergoing cardiac surgery. Data will be collected including demographics, surgery and postoperative complications.; In addition, laboratory data such as coagulation and cytokine will be obtained. Intraoperative monitoring including bispectral index, cerebral oximeter, tissue oxygen saturation \[InspectraTM StO2 (Hutchinson Technology Inc., MN, USA)\], cardiac index \[FloTrac/EV1000 (Edwards Lifesciences, Irvine, CA, USA), VolumeView/EV1000 (Edwards Lifesciences, Irvine, CA, USA), Vigilance II (Edwards Lifesciences, Irvine, CA, USA)\] and mixed venous oxygen saturation will be evaluated.

Trial Locations

Locations (1)

Seoul National University Hospital; 🇰🇷 Seoul, Korea, Republic of