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Ultrasound-guided Blood Sampling Drawing for Microbiological Analysis in the Critically Ill

Use of Ultrasound for Blood Sample Drawing for Microbiological Analysis in Critically Ill Patients:he ECOVEN Feasibility Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06156072
Acronym
ECOVEN
Enrollment
100
Registered
2023-12-05
Start date
2025-06-30
Completion date
2025-12-31
Last updated
2025-03-12

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

Conditions

Diagnosis, Infections, Sepsis, Septic Shock

Brief summary

This study will test the feasibility of ultrasound-guided sterile blood sampling for critically ill patients with suspected sepsis requiring blood culture. The aim of the study is to evaluate the feasibility and safety of the use of ultrasound for blood cultures in a population of patients which can present difficult venous access and requiring more than one venipuncture attempt in general clinical practice

Interventions

DIAGNOSTIC_TESTUltrasound-guided venipuncture

Venipuncture will be performed using ultrasound to identify the most appropriate vessel and guide the puncture

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Lead SponsorOTHER

Study design

Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Adult patients (18 year-old) * admitted to intensive care unit * suspected sepsis requiring blood cultrure

Exclusion criteria

* pregnancy * infections requiring respiratory isolation * burns or skin disease involving arms and/or more than 60% of body surface

Design outcomes

Primary

MeasureTime frameDescription
Number of attempted venipuncturesOne hour after clinical decision of blood culture executionEvaluation of the feasibility of ultrasound-guided venipuncture for blood samples in patients requiring ,microbiological analysis. Feasibility will be evaluated in terms of number of needed attempts of venipuncture

Secondary

MeasureTime frameDescription
Incidence of possible complications (accidental arterial puncture, visible ematoma)One hour after clinical decision of blood culture executionEvaluation of safety of venipuncture in terms of possible complications (accidental arterial puncture, ematoma)
Incidence of contamination of ultrasound-guided venipunctureOne hour after clinical decision of blood culture executionEvaluation of blood sample bacterial contamination compared to blind puncture

Contacts

Primary ContactAntonio M Dell'Anna, M.D.
antoniomaria.dellanna@policlinicogemelli.it3803679256

Outcome results

None listed

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