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Evaluation of respiratory syndrome multi-pathogen rapid detection clinical value

Evaluation of respiratory syndrome multi-pathogen rapid detection clinical value

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081885
Enrollment
Unknown
Registered
2024-03-14
Start date
2024-03-31
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

Upper respiratory infection

Interventions

Treatment group:The rapid detection platform of Accunome nucleic acid was used to quickly obtain the pathogen detection report and guide the clinical medication adjustment in time.
Control group:The routine molecular platform was used to detect respiratory viruses, and the clinician made medication and adjustment according to the test report

Sponsors

Second Hospital of Tianjin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Be at least 18 years old. 2. Hospitalized patients. 3. Accompanied by symptoms of respiratory infection, pathogen testing should be performed according to clinical judgment (and specific indications for clinical confirmation). 4. Informed consent of patient or legal guardian.

Exclusion criteria

Exclusion criteria: 1. Patients using hormone drugs 2. Rheumatoid arthritis patients 3. Patients with severe diabetes 4. Patients with severe hepatic and renal insufficiency 5. Patients with immune insufficiency

Design outcomes

Primary

MeasureTime frame
The timing and adjustment ratio from patient admission to using antimicrobials( including antibiotics and antivirals) according to viral test results ;

Secondary

MeasureTime frame
Compare the difference in reporting time between the DXcellence12 platform and the conventional PCR platform in the laboratory.;Compare the effects of the DXcellence12 platform and the conventional PCR platform in the laboratory on the treatment outcome and cost.;The differences (detection rate, sensitivity and specificity) between the DXcellence12 platform and the conventional PCR platform were compared.;

Countries

China

Contacts

Public ContactYang Cao

Second Hospital of Tianjin Medical University

ttykcaochen@126.com+86 133 7039 6906

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026