CLABSI Prevention With Tissue Adhesive
Recruiting now · Not applicable
Conditions studied: Central-line Associated Blood Stream Infections (CLABSI)
In brief
Our aim is to test the effect of tissue adhesive application at the Central-line exit-site on CLABSI rates in high-risk pediatric congenital heart disease patients.
Key facts
- Study ID
- NCT05721677
- Run by
- Rabin Medical Center
- People needed
- 600
- Starts
- 2023-03-15
- Expected to finish
- 2026-09-15
- Last updated by the study team
- 2024-10-02
Who can join
Age: any, up to 18. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All patients admitted to pediatric cardiac ICU (PCICU) defined as high-risk for CLABSI (any of):
- young age<1y \& Congenital Heart Surgery Mortality Category (STAT\\STS-EACTS) score 2-5
- Risk Adjustment for Congenital Heart Surgery (RACHS) category ≥3
- preoperative length-of-stay (LOS) >7 days
- preoperative ventilator support
- presence of a genetic abnormality
- extracorporeal membrane oxygenation (ECMO) support
You may not qualify if…
- Patients with on-going bacteremia
- patients with pre-existing central-line or peripherally inserted central catheter (PICC)
- parental refusal to participate.
Where it is running
- Schneider's children medical center — Petah Tikva, Israel (enrolling)
Full record on ClinicalTrials.gov
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