Evaluation of Droplet Digital PCR Rapid Detection Method and Precise Diagnosis and Treatment for Suspected Sepsis

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About the study

Sepsis is a significant public health concern worldwide, with high morbidity and mortality. With regard to a targeted antimicrobial treatment strategy, the earliest possible pathogen detection is of crucial importance. Until now, culture-based detection methods represent the diagnostic gold standard, although they are characterized by numerous limitations. Culture-independent molecular diagnostic procedures may represent a promising alternative. In particular, droplet digital PCR (ddPCR) is a novel one-step PCR assay that achieves higher accuracy and sensitivity in detecting causing pathogens in patients with bloodstream infections.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


1.18 years or older


2.Meet 2 of 4 sepsis criteria


  1. Temperature > 38C or < 36C
  2. Heart rate > 90 bpm
  3. Respiratory rate >20 or PaCO2 <32mmHg
  4. WBC >12000/µL or < 4000/µL or > 10% bands

3.Hospitalized patients who have a diagnostic blood culture ordered as standard of care for suspected sepsis


4.Informed Consent by patient or legal representative.


EXCLUSION CRITERIA

Exclusion Criteria:


  • Refusal to participate in the study or Failure to comply with treatment or follow-up time
  • Known breastfeeding or pregnancy
  • The researcher believes that there are any conditions (social or medical) that allow subjects to participate is unsafe. For example, severe anemia or high risk of bleeding,etc., which are not suitable for taking peripheral blood for testing
  • Participating in other clinical studies

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    Study Locations

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    How to Apply


    Contact the study center to learn if this study is a good match for you.

    Study Details


    Contition
    Sepsis,Septic Shock
    Age (in years)
    18+
    Phase
    NA
    Participants Needed
    2000
    Est. Completion Date
    Jun 1, 2023
    Treatment Type
    INTERVENTIONAL

    Sponsor
    Huashan Hospital
    ClinicalTrials.gov NCT Identifier
    NCT05190861
    Study Number
    PROGRESS

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