The Efficiency of the Central Venous Catheter Care Protocol

NCT05705895 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2023-01-31

No results posted yet for this study

Summary

The study aims to evaluate the effectiveness of a central venous catheter (CVC) care protocol, which was created using current guidelines, research results, and expert opinions, on developing CVC-related bloodstream infection in patients with hematopoietic stem cell transplantation (HSCT) until discharge.

Conditions

  • Stem Cell Transplant Complications
  • Central Venous Catheter Exit Site Infection

Interventions

PROCEDURE

CENTRAL VENOUS CATHETER CARE PROTOCOL

Catheter care is provided in line with the CVC care protocol developed by the researcher: * For subsequent catheter care, a transparent sterile catheter cover impregnated with 2% chlorhexidine gluconate will be used. * The entry point of the catheter will be wiped with a disposable sterile skin cleaning applicator containing 2% Chlorhexidine Gluconate and 70% Isopropyl Alcohol, which will be provided by the researchers, and wait for it to dry. * Vein valve/needleless connector will be used. * Effective manual disinfection of needle-free connectors (hubs) will be ensured before each intervention. * Needle-free connectors will be replaced every 96 hours at the latest. * If necessary, the catheter lumen will be washed with a disposable, positive-pressure sterile washing system containing 10 ccs 0.9% sodium chloride to be provided by the investigators. * Pulsatile "give stop give stop" technique will be used in the washing process.

Sponsors & Collaborators

  • Saglik Bilimleri Universitesi Gulhane Tip Fakultesi

    lead OTHER

Principal Investigators

  • Canan PORUCU, MsN, RN · Saglik Bilimleri Universitesi

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-01
Primary Completion
2023-07-01
Completion
2023-12-01

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05705895 on ClinicalTrials.gov