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New catheter lock solution could cut ICU infections
NCT ID NCT07366372
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a taurolidine-based lock solution can prevent infections in central venous catheters used in intensive care. 120 ICU patients received either the taurolidine solution, a tigecycline-heparin mix, or plain saline to lock their catheters. The goal was to see which approach best reduced bacterial growth and bloodstream infections.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- taurolidine-citrate-heparin lock solution
- What this could lead to
- If effective, this could provide a simple way to reduce dangerous catheter infections in ICU patients, potentially saving lives and shortening hospital stays.
- What could go wrong
- This is a small, completed trial with 120 participants, so results may not apply to all ICU settings. The intervention also includes heparin and citrate, which carry bleeding or allergy risks.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
120 people
The number who actually took part.
- Started
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May 2023
- Finished
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Nov 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
21 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Tanta University
Tanta, El-Gharbia, 31527, Egypt
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