ClinicalTrials.gg
RecruitingNCT07183410Updated Oct 9, 2026

Impact of Blood Cultures Drawn From Arterial Lines on the Incidence of Contamination, Detection of Bacteremia, and Blood Culture Volume

An observational study in Bacteremia, sponsored by Meir Medical Center. Recruiting at 1 site in Israel. Open to participants aged 18 Years to 99 Years. Per ClinicalTrials.gov, last updated 2026-10-09.

Sponsored by Meir Medical Center · Observational

From the registry’s dates

  • Started Jan 2026; still recruiting 10 months later.
Updated Oct 9, 2026Now RecruitingSite recruiting status changedGo to Updates ↓
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
1,500
Ages
18 Years to 99 Years
Sex
All
01

Study summary

Taking blood cultures is an important and very common procedure in intensive care units due to the high incidence of sepsis and the need for rapid and accurate identification of bacteremia. However, despite the importance of taking a sufficient volume of blood for the purpose of identifying bacterial growth in the blood, the average blood volume in blood cultures at our institution ranges from 3.5-4 ml per bottle (where the desired volume is 10 ml). Taking an insufficient amount of blood reduces the ability of the bacteriological laboratory to detect bacterial growth and thus may lead to a delay or missed diagnosis of bacteremia, identification of the pathogen, and adjustment of appropriate treatment according to sensitivities.

In intensive care units, most patients are monitored using an arterial catheter, which allows for frequent blood tests without the need to puncture the patient. Following recently published studies that showed that there is no significant difference in the incidence of contamination when taking blood cultures from an arterial catheter compared to a peripheral vein puncture, and in order to improve our ability to identify bacteremia, it was decided to implement a new protocol in the General Intensive Care Unit that includes taking blood cultures from an arterial catheter. According to the new protocol, it was decided that when taking blood cultures from a patient with an arterial catheter, one pair of cultures should be taken from the arterial catheter and another pair from a peripheral vein puncture.

In this study, we would like to examine the contamination rate of blood cultures, the identification of true bacteremia, and the collection of appropriate blood volume and number of blood specimens taken in patients hospitalized in the General Intensive Care Unit at our institution, while analyzing differences between the period before the implementation of the new protocol and the period after the implementation, and differences between cultures taken from an arterial catheter and from a peripheral vein puncture.

02

Conditions studied

  • Bacteremia

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03

In context

Bacteremia

297 studies on the registry are indexed under Bacteremia; 51 are open to participants now.

This study's planned enrollment of 1,500 is above the median of 300 across 125 observational studies indexed under Bacteremia.

Browse Bacteremia studies →

Lead sponsor

Meir Medical Center is the lead sponsor of 401 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All patients admitted to the intensive care unit in our hospital between January 2024 and January 2027 who had blood cultures taken as part of their routine care.

Eligibility criteria

Inclusion Criteria:All patients aged 18-99 years who had blood cultures taken as part of their routine care in the intensive care unit for any reason, from January 2024 to January 2027.

-

Exclusion Criteria:Missing data or patients who did not fullfil the above criteria.

-

05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
1,500 participants (estimated)
Patient registry
No

Groups and cohorts

  • Cultures from arterial line

    From each patient enrolled in the study, two sets of blood cultures will be drawn: one set (2 bottles) from an arterial line and one set from peripheral venous puncture. Each patient will be both the study and the control group for himself: The comparison will be between the arterial line vs. the peripheral vein puncture set. In addition, we will also perform a before and after intervention analysis- to examine whether the implementation of the new protocol improved the rate of appropriate blood culture volume and number of culture drawn from the patient .

    Diagnostic Test: Blood culture taken from an arterial catheter

  • Cultures from peripheral venous puncture

    From each patient enrolled in the study, two sets of blood cultures will be drawn: one set (2 bottles) from an arterial line and one set from peripheral venous puncture. Each patient will be both the study and the control group for himself: The comparison will be between the arterial line vs. the peripheral vein puncture set. In addition, we will also perform a before and after intervention analysis- to examine whether the implementation of the new protocol improved the rate of appropriate blood culture volume and number of culture drawn from the patient .

Interventions

  • Diagnostic testBlood culture taken from an arterial catheter

    Blood culture taken from an arterial catheter (instead of peripheral venous puncture)

06

What researchers measure

Primary outcomes

  1. Contamination and real bacteremia detection rates

    To examine whether there are differences between the contamination rate and the detection rate of true bacteremia between blood cultures from an arterial catheter and blood cultures from a fresh puncture of a peripheral vein.

    Time frame: One week following blood cultures collection

07

Study locations

1 of 1 sites recruiting
08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jan 2026 (actual). Primary completion is estimated for Jan 2028, 24 months after the start.

Of 32 non-industry observational studies under Bacteremia, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 41. This study's planned 24 months is above that.

Counting every sponsor, half of 39 studies reached it within 21 months; a quarter within 11 and three quarters within 38.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 14, 2025
First posted
Sep 19, 2025
StartActual
Jan 1, 2026
Primary completionEst.
Jan 1, 2028
CompletionEst.
Jun 1, 2028
Last update
Oct 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Status
Not yet recruiting→Recruiting
changed Oct 9, 2026
Sites
Meir Medical Center is now Recruiting
Oct 9, 2026
Site contacts
Changed at 1 site. See the sites
Show the site
  • Meir Medical Center · Kfar Saba, IsraelContact added s•••@clalit.org.il · •••2133
Oct 9, 2026
Show all 1 update
  1. Oct 9, 2026
    Not yet recruiting→Recruiting
    Meir Medical Center is now Recruiting
    Site contacts Changed at 1 site. See the sites
    Show the site
    • Meir Medical Center · Kfar Saba, IsraelContact added s•••@clalit.org.il · •••2133
    + 2 other changes: verification date and date precision

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07183410
Responsible party
sara dichtwald (Dr, Meir Medical Center) — Principal investigator
First posted
Sep 19, 2025
Start date
Jan 1, 2026
Primary completion
Jan 1, 2028 (estimated)
Completion
Jun 1, 2028 (estimated)
Last update
Oct 9, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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