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Enhanced Diagnostics of Encephalitis by the use of Next-Generation Sequencing

Conditions
G05
Encephalitis, myelitis and encephalomyelitis in diseases classified elsewhere
Registration Number
DRKS00015835
Lead Sponsor
Westpfalz-Klinikum Kaiserslautern
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
50
Inclusion Criteria

• declaration of consent signed by participant of the clinical trial or the participant’s legal representative
• age > 18 years
• encephalitis: suspected inflammation of brain tissue that is accompanied by neurological dysfunction
• lying or indicated CSF (Cerebrospinal fluid) drainage

Exclusion Criteria

• age < 18 years
• refusal of participation
• transfer from intensive care unit in the first 72h after beginning of clinical trial is very likely
• palliative therapy
• limitation of therapy possible
• death of patient is already in the beginning of clinical trial predictable and seems unavoidable
• patients, that have been included in the study and are retransferred to the intensive care unit, can’t be included a second time
• pregnancy

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
- Microbial detection from CSF-samples (Cerebral spinal fluid) by use of NGS (Next-Generation Sequencing)<br>- Comparison with blood culture<br>- CSF-samples and blood-sampled are drawn at a particular time
Secondary Outcome Measures
NameTimeMethod
- Evaluation of results using SIQ (Sepsis Indicating Quantifier) Score<br>- aim of clinical trial: new approaches for future diagnostics of encephalitis for patients under intensive care <br>
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