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• Comparison of Blood Culture Contamination Rates

Comparison of Blood Culture Contamination Rates Between the Use of Povidine Iodine/Alcohol for Skin Antisepsis and the Use of Chlorhexidine/Alcohol (ChloraPrep) for Skin Antisepsis: An Open-label, Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05576233
Enrollment
500
Registered
2022-10-12
Start date
2023-10-15
Completion date
2024-12-01
Last updated
2023-02-01

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

Conditions

Blood Culture Contamination

Keywords

Blood culture contamination, Chloraprep ( alcohol/ chlorhexidine), Povidine/iodine, Topical disinfectants

Brief summary

In this study, blood culture contamination rates will be compared in patients who used povidine/iodine-alcohol and chlorhexidine/alcohol, which were applied before the blood culture was taken by randomized two methods routinely used in this study.

Detailed description

Detection of the pathogen in blood cultures as soon as possible reduces mortality significantly by providing timely initiation of treatment1. However, when skin antisepsis is not performed properly, an increase in the rate of contamination is observed. In this study, it was planned to compare the contamination rate of two antiseptics, povidine iodine/alcohol and Chlorhexidine/alcohol used as skin antisepsis, in the blood culture taken. Full randomization will be applied in the study. Multiples of 3 of the patients to be included in the study will be included in the Chloraprep group, the remaining patients and multiples of 2 will be included in the povidine/iodine group. . According to the number of samples determined for each institution, patients who came to the outpatient clinic during data collection and accepted to participate in the study will be randomly selected.

Interventions

PROCEDUREdisinfection of the surface that the blood culture is taken

lood cultures can be routinely performed with alcohol/povidine-iodine or alcohol/chlorhexidine. The topical disinfectants used in the two applications are the topical disinfectants included in the guidelines and currently applied in our hospital.

Sponsors

Dr. Behcet Uz Children's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
1 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

* patients who will be hospitalized at SBU Izmir Dr. Patients who are hospitalized in the Pediatric Infection Service of Behçet Uz Pediatrics and Surgery Training and Research Hospital, and who will require blood culture indications will participate in the study If they are willing to

Exclusion criteria

* The patents with central lines will be excluded. * The patient who were transferred from ICU's will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Blood Contamination14 daysThe primary endpoint of the study was to reduce the rate of contamination in blood cultures.

Outcome results

None listed

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