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Clinical Trial

SKİN PROTECTİVE BARRİER FİLM İN CENTRAL VENOUS CATHETER CARE İN INTENSİVE CARE PATİENTS

NCT: NCT07855835 · COMPLETED

NCT IDNCT07855835
StatusCOMPLETED
Start Date2026-01-20
Completion2026-05-15
SponsorBezmialem Vakif University (OTHER)
First posted
Last updated

Brief Summary

This randomized controlled study evaluated the effectiveness of a skin protective barrier film used during central venous catheter (CVC) care in adult intensive care unit patients. A total of 72 patients with a CVC were randomly assigned in a 1:1 ratio to an intervention group or a control group. In the intervention group, a skin protective barrier film was applied during CVC dressing care in addition to the standard care procedure. The control group received standard CVC dressing care without the skin protective barrier film. Patients were followed for seven days. Dressing integrity, skin integrity at the catheter insertion site, presence and type of drainage, signs of infection, and central line-associated bloodstream infection were evaluated. The study aimed to determine whether the use of a skin protective barrier film during CVC care contributes to maintaining skin and dressing integrity and affects catheter-related complications.

Frequently Asked Questions

What is SKİN PROTECTİVE BARRİER FİLM İN CENTRAL VENOUS CATHETER CARE İN INTENSİVE CARE PATİENTS?

SKİN PROTECTİVE BARRİER FİLM İN CENTRAL VENOUS CATHETER CARE İN INTENSİVE CARE PATİENTS is a clinical trial registered under NCT07855835. Current status: COMPLETED.

What is the status of NCT07855835?

The current status of NCT07855835 (SKİN PROTECTİVE BARRİER FİLM İN CENTRAL VENOUS CATHETER CARE İN INTENSİVE CARE PATİENTS) is: COMPLETED.

When did SKİN PROTECTİVE BARRİER FİLM İN CENTRAL VENOUS CATHETER CARE İN INTENSİVE CARE PATİENTS start?

SKİN PROTECTİVE BARRİER FİLM İN CENTRAL VENOUS CATHETER CARE İN INTENSİVE CARE PATİENTS started on 2026-01-20.

Related Devices

K242429CentroVena Central Venous Catheter (CVC) with the CentroVena One Insertion SystemBecton Dickinson Inc. (Bd) K241946PeritX™ 1L Drainage Kit (90-1010); PeritX™ 2L Drainage Kit (90-2010); PeritX™ Peritoneal Catheter Kit (50-9000C); PeritX™ Peritoneal Catheter and Starter Kit (50-9900C); PeritX™ Peritoneal Catheter Mini Kit (50-9050A); PleurX™ Low Profile Catheter Mini Kit (50-8050); Valve Cap (50-7235A); PeritX™ Valve Kit (50-7272); Catheter Access Kit (50-7280A); Lockable Drainage Line (50-7245A); Lockable Drainage Line Kit (50-7265A); PleurX™ Supplemental Insertion Kit (50-7262); Procedure Pack (50-Bard Peripheral Vascular, Inc.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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