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A Study to Evaluate a New Jaundice Stick Test

NCT02926131 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 180

Last updated 2018-10-02

No results posted yet for this study

Summary

This is an observational prospective study. The main purpose is to evaluate the stability of the Bilistick system in a humid and hot climate compared to the quantitative test for serum bilirubin (SBR) measurement currently used, the BR-501 total bilirubin meter, kept in a controlled environment.

The secondary aim is to assess the operational feasibility of the Bilistick system in a tropical limited-resource setting, when used by locally trained nurses.

Conditions

  • Jaundice
  • Serum Bilirubin

Interventions

OTHER

Blood sampling

* One full capillary tube (50µl blood) will be used to measure the Hct level and the routine SBR using the BR-501 bilirubin meter machine (non-study procedure). * An additional half- filled capillary tube (25µl blood) will be used for the SBR measurement with the Bilistick system

Sponsors & Collaborators

  • Shoklo Malaria Research Unit

    collaborator OTHER

  • University of Oxford

    lead OTHER

Principal Investigators

  • Professor Rose McGready, MD · Shoklo Malaria Research Unit (SMRU)

Eligibility

Min Age
1 Day
Max Age
28 Days
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-01-25
Primary Completion
2017-12-11
Completion
2017-12-11

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02926131 on ClinicalTrials.gov