Wounds and InjuriesNCT06237283
Effects of Early Postoperative Showering After Coronary Artery Bypass Grafting Using Bilateral Internal Thoracic Artery
A study testing Early shower in people with Wounds and Injuries and Wound Infection, run by Sejong General Hospital at 1 site in South Korea.
Trial summary
The study to evaluate effects of early postoperative showering after coronary artery bypass grafting using bilateral internal thoracic artery Read more about this study
- Who is it for?
- Ages 19 years and older
- Conditions the study is for
- Wounds and Injuries, Wound Infection
- What is being tested?
- Early shower
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 200 participants
- Where
- 1 siteSouth Korea
- Study dates
- 3 Jan 2024to 1 Mar 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 19 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country.
South Korea1 site, 1 recruiting
- Recruiting
Bucheon Sejong Hospital
Bucheon-si, Gyeonggi-do, 14754
HEEMOON LEE, 82-10-9083-6249, rhythmists@gmail.com
About this study
The study to evaluate effects of early postoperative showering after coronary artery bypass grafting using bilateral internal thoracic artery
- Conditions
- Wounds and Injuries, Wound Infection
- Being tested
- Early shower
- Medical subject headings
- Wounds and Injuries, Wound Infection
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Early showerBehavioural
Start shower after drain removal
| Study group | Role | What they receive |
|---|---|---|
| Early shower | Experimental | Start shower after drain removal Receives: Behavioral: Early shower |
| Late shower | No intervention | Start shower after wound stitches are removed |
What is being measured
The primary outcome is the main question the study is designed to answer.
Rate of deep sternal wound infection
Measured: until 1 months after discharge
Rate of superficial sternal wound infection
Measured: until 1 months after discharge
Rate of wound dehiscence
Measured: until 1 months after discharge
Secondary outcomes (6)
Patient satisfaction
questionnaire
Measured: at 1st outpatient clinic visit
Rate of mortality
Measured: until 1 months after discharge
Rate of stroke
Measured: until 1 months after discharge
Rate of respiratory complications
Measured: until 1 months after discharge
Rate of bleeding requiring reoperation
Measured: until 1 months after discharge
Rate of low cardiac output syndrome
Measured: until 1 months after discharge
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Feb 2024
- Study start3 Jan 2024
- Primary completion1 Mar 2025 (estimated)
- Study completion1 Mar 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Wounds and InjuriesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Sejong General Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06237283
- Sponsor's protocol ID
- BSH 2023-09-005
- Status last verified
- Jan 2024
- First submitted
- 23 Jan 2024
- Last updated
- 2 Feb 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 2 Feb 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Early Postoperative Showering After Coronary Artery Bypass Grafting Using Bilateral Internal Thoracic Artery
- ClinicalTrials.gov ID
- NCT06237283
- Acronym / sponsor ID
- BSH 2023-09-005
- Conditions
- Wounds and Injuries, Wound Infection
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- Sejong General HospitalUniversity, hospital or other
- Study start
- 3 Jan 2024 (actual)
- Primary completion
- 1 Mar 2025 (estimated)
- Study completion
- 1 Mar 2025 (estimated)
- First posted
- 1 Feb 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The study to evaluate effects of early postoperative showering after coronary artery bypass grafting using bilateral internal thoracic artery
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Early shower | Experimental | Behavioral: Early showerStart shower after drain removal |
| Late shower | No intervention | –Start shower after wound stitches are removed |
Who may qualify
- Ages
- 19 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- 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
Key exclusion criteria (6 listed)
- Concomitant operation
- Redo-surgery
- prolonged intensive care unit stay (more than 4 days) due to serious complications after surgery
- open wounds
- active infection
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Early showerStart shower after drain removal | Behavioural | Early shower |
Primary outcome
Rate of deep sternal wound infection
Time frame: until 1 months after discharge
Rate of superficial sternal wound infection
Time frame: until 1 months after discharge
Rate of wound dehiscence
Time frame: until 1 months after discharge
6 secondary outcomes
Patient satisfaction
Time frame: at 1st outpatient clinic visit
Rate of mortality
Time frame: until 1 months after discharge
Rate of stroke
Time frame: until 1 months after discharge
Rate of respiratory complications
Time frame: until 1 months after discharge
Rate of bleeding requiring reoperation
Time frame: until 1 months after discharge
Rate of low cardiac output syndrome
Time frame: until 1 months after discharge
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Feb 2024.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Early shower in people with Wounds and Injuries and Wound Infection, run by Sejong General Hospital at 1 site in South Korea.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 2 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact HEEMOON LEE (82-10-9083-6249, rhythmists@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Rate of deep sternal wound infection (time frame: until 1 months after discharge). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Feb 2024.