Skip to content

The Right Amount of Purge Useful for Blood Sampling on PiccLine (PiccLine)

The Right Amount of Purge Useful for Blood Sampling on PiccLine

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05763186
Acronym
PiccLine
Enrollment
66
Registered
2023-03-10
Start date
2024-05-18
Completion date
2026-05-31
Last updated
2025-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hematology

Keywords

PiccLine, blood collection, purge

Brief summary

An increasing number of patients are receiving central lines, including PiccLine systems for the administration of therapeutics and nutrition. Although these systems are not theoretically intended for blood collection, nurses prefer them as a puncture site when they are in place in their patients, saving them from further peripheral puncture in people who generally do not have optimal venous capital. It is essential to purge the tubing in place in the patient and filled with infusion solution before drawing blood. Although the dead volume of the tubing used does not exceed 2mL, the volume of purging required before filling tubes for the laboratory appears to be much greater. Anecdotal evidence suggests a useful volume of 20ml but this has never been clearly demonstrated. In addition, the Biochemistry laboratory regularly sees blood samples diluted with perfusion solution, as evidenced by biochemical assays, leading to the cancellation of analyses received in the laboratory and a new sample being taken. This increases blood spoliation for these often already anaemic patients. There is no consensus in the literature on recommendations for such sampling in PiccLine patients: * The CLSI1 (Clinical and Laboratory Standart Institute), a non-governmental organisation, issued sampling recommendations in 2017 that were taken up by Becton Dickinson2, a supplier of blood collection tubes. These recommendations include: * Rinse with 10 ml of 0.9% NaCl * Then a purge of 3 to 11 ml (depending on the analysis sought) * English-language articles3,4,5,6,7 show purge volumes ranging from 3 to 6 ml with significantly different sampling methods (rinsing or not). The investigators therefore note a discrepancy between the sampling practices of the university hospital and the recommendations of the CLSI. In fact, the investigators noted a lack of rinsing prior to purging, which could explain the difference between 20 and 3 ml. This raises the issue of protocolisation of this type of sampling in order to standardise practices. A consultation of other hospitals, carried out beforehand, enabled us to note that French practices are not in agreement with these recommendations. The management of the Rennes University Hospital as well as the Haute Autorité de Santé were contacted in order to confirm that no normative document had been published or was being drafted on this subject. The fields of study are: sampling practices on PiccLine, the pre-analytical phase in medical biology.

Interventions

OTHERSampling

Comparison of the results of the biological examinations obtained on the 6 tubes collected on the PiccLine with the results of the biological examinations obtained on the peripheral sample.

OTHERSampling and rinsing

Comparison of the results of the biological examinations obtained on the 6 tubes collected on the PiccLine with the results of the biological examinations obtained on the peripheral sample.

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age ≥ 18 years 2. Carrier of PiccLine one way polyurethane 3. Hospitalized in a clinical hematology unit This criterion minimises patient and practice heterogeneity. 4. PiccLine placement not older than 48 hours 5. Injection of at least one solution 6. Affiliated to a social security scheme 7. Having signed a free, informed and written consent

Exclusion criteria

1. Anemia below the transfusion threshold (hemoglobin level \< 7 g/dL) in relation to the patient's pathology 2. Parenteral nutrition 3. Peripheral venous sampling not possible (insufficient venous capital) 4. Protected person (adult subject to legal protection (safeguard of justice, curatorship, guardianship), person deprived of liberty, pregnant woman (declarative), breastfeeding woman and minor).

Design outcomes

Primary

MeasureTime frame
Lowest purge volume to obtain a biological result in the PiccLine sample that matches the peripheral sample taken from the same patient at the same time for the following assays: - Sodium, potassium and chlorine - Creatinine - Glucoseduring 2 days follow-up

Countries

France

Contacts

Primary ContactNicolas Mevel
dri@chu-rennes.fr02 99 28 25 55
Backup ContactAnne Ganivet
anne.ganivet@chu-rennes.fr02 99 28 25 55

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026