Can fewer dressing changes make PICC lines safer?
NCT ID NCT07802314
First seen Sep 03, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This trial compares different care schedules for peripherally inserted central catheters (PICCs), which are long-term IV lines. Researchers want to see if extending the time between dressing changes, while using special securement and antiseptic dressings, reduces infections and other complications. The study includes 240 adults who need a PICC and can manage their own daily activities. Participants will be assigned to one of several care routines, and the team will track complications like phlebitis, bloodstream infections, and accidental line removal.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Different care frequencies for peripherally inserted central catheters (PICCs), including use of SecurAcath securement and chlorhexidine dressings
- What this could lead to
- If successful, this could establish safer, less frequent care routines for PICC lines, reducing infections and other complications while improving patient comfort.
- What could go wrong
- The trial is relatively small and focuses on a specific care protocol, so results may not apply to all hospitals or patient groups. Complications can still occur despite optimized care.
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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 240 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Jun 2028
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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18 years and older
- 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.
Inclusion Criteria: * be over 18 years of age * accept participation in the study * independent patient in the care and management of activities of daily living Exclusion Criteria: * patient over 18 years of age * patient with functional or cognitive limitation * patient with mild, moderate or high level of dependence * patient does not accept to perform the study * patient with device withdrawal prior to 14 days of duration
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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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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