SIMBLE-FIELD: Diagnostic Evaluation Study of the BactInsight Blood Culture System in West-Africa

Sponsor
Institute of Tropical Medicine, Belgium (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05722184
Collaborator
Reactivos para Diagnóstico, S.L. (Other), University Ghent (Other), Université Libre de Bruxelles (Other), Commissariat A L'energie Atomique (Other), Centre Hospitalier Universitaire Yalgado Ouédraogo (Other), Centre National Hospitalier et Universitaire de Pneumo-Phtisiologie de Cotonou (Other), European and Developing Countries Clinical Trials Partnership (EDCTP) (Other)
1,347
21.1

Study Details

Study Description

Brief Summary

Diagnosis of bloodstream infections (BSI) is done by sampling blood in blood culture bottles that are checked for growth in the microbiology laboratory. In LRS, microbiology laboratories are however scarce, and BSI cannot be diagnosed, resulting in overuse of antibiotics which fuels AMR. For diagnosis of BSI, so-called manual blood culture (equipment-free) systems are used in LRS, with daily visual inspection for growth. Compared to automates, manual systems are less sensitive, and growth is slower; in addition, training and experience are needed before laboratory staff is competent to detect growth when inspecting the blood culture bottles.

A simplified blood culture system could enable expanded use of blood cultures in LRS and would thus improve BSI treatment. Ongoing research at the Institute of Tropical Medicine, in collaboration with Ghent University has resulted in a novel, simple, cheap, open-access and robust blood culture system, the Bactinsight blood culture system. This system consists of two modules. Firstly, a portable, battery-operated measurement device (turbidimeter), which monitors and detects bacterial growth in blood culture bottles based on the turbidity of the culture medium caused by bacterial growth. Secondly, optimized blood culture bottles have been developed. A second step in blood cultures is the identification of the causing organism. Researchers at LETI (Grenoble, France) have developed a lensfree microscope, which simplifies and expedites identification of the causative organisms, improving patient's diagnosis and more directed antibiotic treatment. The lensfree microscope is an additional module for the Bactinsight blood culture system.

In SIMBLE, the Bactinsight blood culture system will be evaluated against reference systems in two phases. During the optimization phase in Belgium, the performance of Bactinsight turbidimeter + lensfree microscope will be tested in a reference hospital laboratory. In parallel, an in vitro laboratory evaluation of the Bactinsight blood culture system (turbidimeter + blood culture bottles + lensfree microscope) will be done using spiked blood cultures. In the field-testing phase, the ease-of-use, acceptability, adoptability and performance of Bactinsight blood culture system will be evaluated in three hospitals in Benin and Burkina Faso. The blood culture bottles used for this study will be manufactured in a production facility in Benin, that will be installed at the start of the project.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: BactInsight blood culture system

Study Design

Study Type:
Observational
Anticipated Enrollment :
1347 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Diagnostic Evaluation Study of the BactInsight Blood Culture System in West-Africa
Anticipated Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
CNHU-HKM

BactInsight system compared to BacT/ALERT® 3D

Diagnostic Test: BactInsight blood culture system
A battery-operated measurement device (turbidimeter), which monitors and detects bacterial growth in blood culture bottles based on the turbidity of the culture medium caused by bacterial growth, in combination with optimized blood culture bottles.

Hôpital Saint Jean de Dieu, Boko

BactInsight system compared to manual blood culture system (visual inspection)

Diagnostic Test: BactInsight blood culture system
A battery-operated measurement device (turbidimeter), which monitors and detects bacterial growth in blood culture bottles based on the turbidity of the culture medium caused by bacterial growth, in combination with optimized blood culture bottles.

Centre Hospitalier Universitaire Yalgado Ouédraogo

BactInsight system compared to BacTec FX40

Diagnostic Test: BactInsight blood culture system
A battery-operated measurement device (turbidimeter), which monitors and detects bacterial growth in blood culture bottles based on the turbidity of the culture medium caused by bacterial growth, in combination with optimized blood culture bottles.

Outcome Measures

Primary Outcome Measures

  1. Time-to-actionable result [Within 8 days]

    The paired Wilcoxon signed rank test will be used to compare the location of the distribution of time-to-actionable result measurements between the two groups for those with a positive blood culture result. BactInsight versus manual system: Time-to-actionable result is compared between both groups with the Wilcoxon signed rank test at the 5% significance level. BactInsight versus automated system: The non-inferiority margin equals 12 hours. Non-inferiority is shown if the upper limit of the two-sided 95% confidence interval for the median of the differences from the Wilcoxon signed rank test is lower than 12h i.e. 12 is excluded from the non-parametric confidence interval.

Secondary Outcome Measures

  1. Time-to-detection [Within 8 days]

    The paired Wilcoxon signed rank test will be used to compare the location of the distribution of time-to-detection measurements between the two groups for those with a positive blood culture result.

  2. Yield [2 years]

    The McNemar's test will be used to compare the yield between the BactInsight system and the manual reference system at the 5% significance level in order to detect if there is a statistically significant difference between the paired binary data in terms of proportions. o The difference in yield between the BactInsight system and the automated system will be compared to a non-inferiority margin of 15%. Non-inferiority is shown if the lower limit of the two-sided 95% confidence interval is larger than -0.15 i.e. if -0.15 is excluded from the confidence interval. A non-inferiority margin of 15% was chosen as reasonable based on clinical and practical arguments.

  3. Diagnostic performance [2 years]

    Sensitivity and specificity will be calculated for the BactInsight system compared to the composite reference standard, based on the combined result from the components tests i.e. the BactInsight and reference system in use.

Other Outcome Measures

  1. Yield - Antibiotic use [2 years]

    Test whether yield differs in case of antibiotic use (yes/no) within 48 hours prior to blood culture sampling: Pearson Chi-square test (or Fisher exact test in case of small sample size).

  2. Yield - V blood sampled [2 years]

    Test whether yield differs with different volumes of blood sampled (e.g. 5-8 ml; 8-10 ml; 10-15 ml): Pearson Chi-square test (or Fisher exact test in case of small sample size).

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • With indications for blood culture sampling and for whom collection of a blood culture sample is part of standard clinical practice

  • Willing and able to provide written informed consent (assent for minors)

Exclusion Criteria:
  • none

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Institute of Tropical Medicine, Belgium
  • Reactivos para Diagnóstico, S.L.
  • University Ghent
  • Université Libre de Bruxelles
  • Commissariat A L'energie Atomique
  • Centre Hospitalier Universitaire Yalgado Ouédraogo
  • Centre National Hospitalier et Universitaire de Pneumo-Phtisiologie de Cotonou
  • European and Developing Countries Clinical Trials Partnership (EDCTP)

Investigators

  • Principal Investigator: Barbara Barbé, Instituut voor Tropische Geneeskunde

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Institute of Tropical Medicine, Belgium
ClinicalTrials.gov Identifier:
NCT05722184
Other Study ID Numbers:
  • SIMBLE-FIELD
First Posted:
Feb 10, 2023
Last Update Posted:
Feb 14, 2023
Last Verified:
Feb 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Keywords provided by Institute of Tropical Medicine, Belgium
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 14, 2023