New trial aims to slash deadly bloodstream infections from hospital tubes

NCT ID NCT07587593

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

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

About 2,500 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Dec 2026

An estimate. Start dates often move.

Expected to finish

Dec 2031

An estimate. End dates often move.

Lead sponsor

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

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

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

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

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  1. The official record

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