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Droplet Digital PCR Combines With Transcriptome Analysis in Early Warning of Sepsis in the Emergency Department

Clinical Evaluation of Droplet Digital Polymerase Chain Reaction in Combination With Transcriptome Analysis in Early Warning of Sepsis in the Emergency Department: A Multicenter Prospective Observational Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06028178
Enrollment
360
Registered
2023-09-08
Start date
2024-05-01
Completion date
2026-12-31
Last updated
2024-04-17

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

Conditions

Emergent Infections, Treatment, Sepsis

Keywords

Droplet digital PCR, Transcriptomic molecular target assay

Brief summary

Rapid identification of pathogens and early warning of host response are key to improve the prognosis of sepsis. Establishing a comprehensive identification system based on pathogen identification and host immune status is an effective way to achieve early warning stratification of patients with infections in the emergency department. This prospective multicenter clinical study will combine droplet digital PCR (ddPCR) and transcriptomic molecular target assay for validation in patients with suspected sepsis in the emergency department. The purpose is to (1) compare the efficacy of ddPCR with blood culture for early diagnosis and prognosis; (2) assess the diagnostic value of transcriptomic molecular targets based on 29 messenger RNA for the presence or absence of infection as well as infectious agents, and to evaluate their efficacy for prognosis; and (3) assess the diagnostic and therapeutic monitoring value of ddPCR combined with transcriptome analysis methods.

Detailed description

Rapid identification of pathogens and early warning of host response are key to improve the prognosis of sepsis. Establishing a comprehensive identification system based on pathogen identification and host immune status is an effective way to achieve early warning stratification of patients with infections in the emergency department. Therefore, based on our preliminary single-center study, this prospective multicenter clinical study will combine droplet digital PCR (ddPCR) and transcriptomic molecular target assay for validation in patients with suspected sepsis in the emergency department. The purpose is to (1) compare the efficacy of ddPCR with blood culture for early diagnosis and prognosis; (2) assess the diagnostic value of transcriptomic molecular targets based on 29 messenger RNA for the presence or absence of infection as well as infectious agents, and to evaluate their efficacy for prognosis; and (3) assess the diagnostic and therapeutic monitoring value of ddPCR combined with transcriptome analysis methods. In a word, this study will be undertaken to assess the diagnostic and therapeutic monitoring value of early warning models for sepsis in emergency department and to promote them to improve the identification ability of emergency infections.

Interventions

DIAGNOSTIC_TESTDroplet digital PCR

Droplet digital PCR has potential in resolving polymicrobial infection because it simultaneously achieves unprecedented high sensitivity , high specificity, and absolute quantification without the need for a standard curve.

Sponsors

Shanghai East Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* age ≥ 18 years, regardless of sex * MSS≥2 score * written informed consent obtained

Exclusion criteria

* Age \< 18 years, regardless of sex * Patient's ICU length of stay \<24 hours * Malignant tumor, HIV patients or any terminal-stage disease * Known pregnancy or lactation * Participation in other clinical trials * Inadequate clinical information or missing experimental data * No signed informed consent obtained

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic efficiency of ddPCR combined with transcriptomic analysis in suspected sepsis7daysDiagnostic efficiency of ddPCR combined with transcriptomic analysis for suspected sepsis in the emergency medicine
Prognostic value of ddPCR combined with transcriptomic analysis in suspected sepsis28 daysPrognostic value of ddPCR combined with transcriptomic analysis for suspected sepsis in the emergency medicine

Secondary

MeasureTime frameDescription
7-day all-cause mortality rate7 daysEvaluation of combined examination by ddPCR and transcriptomic analysis for the evaluation of the prognosis of the sepsis.
28-day all-cause mortality rate28 daysEvaluation of combined examination by ddPCR and transcriptomic analysis for the evaluation of the prognosis of the sepsis.
90-day all-cause mortality rate90 daysEvaluation of combined examination by ddPCR and transcriptomic analysis for the evaluation of the prognosis of the sepsis.
Antimicrobial Resistance and antibiotic application7 daysEvaluation of combined examination by ddPCR and transcriptomic analysis for the the value of guiding clinical drug therapy.

Outcome results

None listed

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