Surgical Wound Infection Prevention Bundle in Patients Undergoing Coronary Bypass Graft Surgery
NCT ID: NCT07003750
Last Updated: 2025-06-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
NA
200 participants
INTERVENTIONAL
2025-07-01
2026-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Incidence and Risk Factors of Surgical Site Infections After Coronary Artery Bypass Grafting Surgery
NCT07130422
Risk Factors for Deep Sternal Wound Infection After Coronary Artery Bypass Grafting
NCT07043296
Continuous Comprehensive Nursing for Post-CABG Recovery
NCT07062432
Effects of Triclosan-coated Sutures in Cardiac Surgery
NCT01212315
On-pump Versus Off-pump Coronary Artery Bypass Grafting , Short Term Outcomes , Sohag Experience
NCT06069986
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
group 1
* Preoperative:
1. Nightly CHG baths
2. Mupirocin nasal ointment twice daily for 2 to 5 days prior to surgery
3. Hair removal with clippers
* Intraoperative:
1. Skin antisepsis with CHG solution
2. Standardized IV antibiotic doses at the following time points :within 5 to 60 minutes of the initial surgical incision, with initiation of cardiopulmonary bypass ,and every 3 hours intraoperatively for the duration of the case.
* Postoperative :
1. The occlusive sternal dressing applied at time of chest closure and removed 48 hours postoperatively then daily dressing thereafter.
2. Daily postoperative linen change and minimize sternotomy exposure to home blankets
Surgical wound infection prevention bundle
utilization of locally customized surgical wound infection bundle to prevent and or control of infection in patients undergoing CABG surgery
group 2
* Preoperative:
1. Preoperative water and soap bath
2. Hair removal with razor
* Intraoperative:
1. Skin antisepsis with betadine solution
2. One dose of antibiotic just before skin incision
* Postoperative:
1. The occlusive sternal dressing removed 72 hours postoperatively then daily dressing
2. No specific concerns about linens change and home blankets exposure
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Surgical wound infection prevention bundle
utilization of locally customized surgical wound infection bundle to prevent and or control of infection in patients undergoing CABG surgery
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Sohag University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mohamed Ragab Mostafa
cardiothoracic surgery resident
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
soh-Med--25-4-05MS
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.