New trial aims to slash deadly bloodstream infections from hospital tubes
NCT ID NCT07587593
First seen Jun 27, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This study will test different methods to prevent infections and other problems from central lines (tubes placed in large veins) in 2,500 patients. It compares special antimicrobial caps and a skin anchor device against standard care. The goal is to find the best ways to keep patients safe from serious bloodstream infections.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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About 2,500 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2031
An estimate. End dates often move.
- 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
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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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.
Core inclusion Criteria: * The patient has or requires a CVAD, including a PICC, a non-tunnelled or tunnelled CVC, or a totally implanted venous access port. * Patient is less than 18 years old and paediatric recruitment has not been approved at the site. Securement Domain exclusion criteria: * Central line-associated bloodstream infection (CLABSI) currently suspected associated with any vascular access device (peripheral or central) that is in situ. * CLABSI diagnosed from any vascular access device currently in situ within the past 7 days or being actively treated with antimicrobials. * Participants with an estimated life expectancy of \<30 days OR who have commenced a documented end-of-life, terminal-care, or comfort-care pathway. * Participants who have previously been randomised for the same CVAD. * Participants who have been randomised three times. * SecurAcath® cannot be applied in accordance with manufacturer instructions and local policy. * The participant has compromised skin integrity at the current or intended insertion site, including active infection, inflammation, erosion, ulceration, or pre-existing exit-site injury. Connectors/Caps Domain exclusion criteria: * Central line-associated bloodstream infection (CLABSI) currently suspected associated with any vascular access device (peripheral or central) that is in situ. * CLABSI diagnosed within the past 14 days or CLABSI being actively treated with antimicrobials, associated with any vascular access device currently in situ. * Participants with an estimated life expectancy of \<30 days OR who have commenced a documented end-of-life, terminal-care, or comfort-care pathway. * Participants who have previously been randomised for the same CVAD. * Participants who have been randomised three times. * Known or suspected hypersensitivity or a confirmed allergy to chlorhexidine. Cancer stratum inclusion criteria: * Confirmed diagnosis of a solid tumour OR * Confirmed diagnosis of a haematological malignancy. OR * Bone marrow failure syndrome requiring systemic therapy, immunosuppression, or haematopoietic stem cell transplantation. Kidney stratum exclusion criteria: * Confirmed diagnosis of kidney failure treated with haemodialysis AND * CVAD expected to remain in place for \>14 days.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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