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NCT06237283 Clinical Trial

Effects of Early Postoperative Showering After Coronary Artery Bypass Grafting Using Bilateral Internal Thoracic Artery

Wounds and Injuries Clinical Trial

Official title:
Effects of Early Postoperative Showering After Coronary Artery Bypass Grafting Using Bilateral Internal Thoracic Artery

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06237283
Other study ID # BSH 2023-09-005
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 3, 2024
Est. completion date March 1, 2025

Study information
Verified date January 2024
Source Sejong General Hospital
Contact HEEMOON LEE
Phone 82-10-9083-6249
Email rhythmists@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study to evaluate effects of early postoperative showering after coronary artery bypass grafting using bilateral internal thoracic artery

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date March 1, 2025
Est. primary completion date March 1, 2025
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - Age > 18 - Patients who underwent coronary bypass grafting with bilateral internal thoracic artery through median sternotomy - Patients whose all drains or pacing wires are removed Exclusion Criteria: - Concomitant operation - Redo-surgery - prolonged intensive care unit stay (more than 4 days) due to serious complications after surgery - open wounds - active infection - prolonged drains

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Early shower
Start shower after drain removal

Locations
Country Name City State
Korea, Republic of Bucheon Sejong Hospital Bucheon Gyeonggi-do

Sponsors (1)
Lead Sponsor Collaborator
Sejong General Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Rate of deep sternal wound infection until 1 months after discharge
Primary Rate of superficial sternal wound infection until 1 months after discharge
Primary Rate of wound dehiscence until 1 months after discharge
Secondary Patient satisfaction questionnaire at 1st outpatient clinic visit
Secondary Rate of mortality until 1 months after discharge
Secondary Rate of stroke until 1 months after discharge
Secondary Rate of respiratory complications until 1 months after discharge
Secondary Rate of bleeding requiring reoperation until 1 months after discharge
Secondary Rate of low cardiac output syndrome until 1 months after discharge
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