Effects of Early Postoperative Showering After Coronary Artery Bypass Grafting Using Bilateral Internal Thoracic Artery
1 other identifier
interventional
200
1 country
1
Brief Summary
The study to evaluate effects of early postoperative showering after coronary artery bypass grafting using bilateral internal thoracic artery
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 3, 2024
CompletedFirst Submitted
Initial submission to the registry
January 23, 2024
CompletedFirst Posted
Study publicly available on registry
February 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2025
CompletedFebruary 2, 2024
January 1, 2024
1.2 years
January 23, 2024
January 31, 2024
Conditions
Outcome Measures
Primary Outcomes (3)
Rate of deep sternal wound infection
until 1 months after discharge
Rate of superficial sternal wound infection
until 1 months after discharge
Rate of wound dehiscence
until 1 months after discharge
Secondary Outcomes (6)
Patient satisfaction
at 1st outpatient clinic visit
Rate of mortality
until 1 months after discharge
Rate of stroke
until 1 months after discharge
Rate of respiratory complications
until 1 months after discharge
Rate of bleeding requiring reoperation
until 1 months after discharge
- +1 more secondary outcomes
Study Arms (2)
Early shower
EXPERIMENTALStart shower after drain removal
Late shower
NO INTERVENTIONStart shower after wound stitches are removed
Interventions
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bucheon Sejong Hospital
Bucheon-si, Gyeonggi-do, 14754, South Korea
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 23, 2024
First Posted
February 1, 2024
Study Start
January 3, 2024
Primary Completion
March 1, 2025
Study Completion
March 1, 2025
Last Updated
February 2, 2024
Record last verified: 2024-01