Nurses take the lead: can they master PICC placement?
NCT ID NCT06979128
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study in Poland is checking how well a specially trained nursing team can insert PICCs (a type of long-term IV line) in 200 adult patients who need them for treatments like chemotherapy or nutrition. The main goal is to see how often they succeed on the first try. It's an observational study, meaning it just watches what happens without testing a new drug or device.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could show that nurse-led teams can safely and effectively place PICCs, potentially improving access to this procedure.
- What could go wrong
- This is an observational study with no new treatment, so it won't directly change patient care. Results may not apply to all hospitals or countries.
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.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2025
- Expected to finish
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May 2026
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.
Who is studied
All subjects patients who require a PICC
- 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: * Age \>18 years * Intravenous therapy with solutions requiring central vein cannulation (irritant drugs, extreme pH \<5 and \>9, osmolarity \> 600 mOsm/l), e.g., chemotherapy, parenteral nutrition with osmolarity \>900 mOsm/l * Difficult intravenous access with multiple blood collection * Ability to consent to participate in the study * Consent to participate in the study Exclusion Criteria: * Presence of central venous catheter, such as. centrally inserted central catheter or totally implanted vascular device * Indication of another type of vascular access device * Lack of veins suitable for cannulation of the arm * Infection, burns or other skin lesion on the upper extremities (involving the site of planned catheter insertion and attachment) * Pregnancy (confirmed by history and review of medical records or confirmed by positive human chorionic gonadotropin (hCG) determination in urine or plasma) * Lack of patient consent to participate in the study * Lack of capacity to consent to participate in the study * No physician present to supervise the procedure
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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
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Medical University of Warsaw
Warsaw, Poland
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