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Efficacy of Taurolidine Containing Lock Solution for Prevention of Central Venous Catheter Infection in ICU Patients

The Efficacy of Taurolidine Containing Lock Solution for Prevention of Central Venous Catheter Infection in ICU Patients

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07366372
Enrollment
120
Registered
2026-01-26
Start date
2023-05-01
Completion date
2024-11-01
Last updated
2026-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Central Venous Catheter Infection, Intensive Care Unit, Lock Solution, Prevention, Taurolidine

Brief summary

This study aimed to assess effectiveness of a taurolidine based lock solution in preventing the infections of central venous catheter (CVC) in intensive care unit (ICU) cases.

Detailed description

The central venous catheter (CVC) is highly frequent in the intensive care unit (ICU), with an average use rate between 32% and 80% among adult ICU patients. The utilization of CVC in ICUs has escalated over the past decade, accompanied by a corresponding increase in problems related to their usage. Taurolidine is a nontoxic substance having antibacterial impacts counter to mutually gram-positive and -negative bacteria, additionally to fungus. It decreases biofilm development and doesn't develop resistance to antibiotics, since it serves as an antiseptic rather than an antibiotic Consequently, it may function as a locking mechanism.

Interventions

DRUGSaline

Central venous catheters (CVCs) were locked with 2ml saline as a control group.

DRUGTigecycline and heparin

Central venous catheters (CVCs) were locked with 2ml of a solution comprising tigecycline 5mg/ml and heparin 500 IU/ml.

DRUGTaurolidine-citrate-heparin

Central venous catheters (CVCs) were locked with 2ml of a solution containing taurolidine-citrate-heparin (1.35% taurolidine, 4% citrate, and 500 IU/ml heparin).

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 21 years. * Both genders. * Patients admitted to the intensive care unit (ICU) requiring central venous catheter insertion.

Exclusion criteria

* Cases with active infections, hemorrhage or bleeding disorders, infections within insertion place. * History of allergy to taurolidine, tigecycline, heparin, and citrate.

Design outcomes

Primary

MeasureTime frameDescription
Positive bacterial growth30 days after the procedurePositive bacterial growth of a swab was recorded.

Secondary

MeasureTime frameDescription
Assessment of catheter-related bloodstream infection30 days after the procedureAssessment of catheter-related bloodstream infection was recorded.
Assessment of central venous catheter infection30 days after the procedureAssessment of central venous catheter (CVC) infection was recorded.
Lenght of intensive care unit stay30 days after the procedureLenght of intensive care unit (ICU) stay was recorded.
Incidence of mortality30 days after the procedureIncidence of mortality was recorded.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026