Pure Global

Assessement of Microcirculation With NIRS Predicts Sepsis Development in Patients With Severe Covid-19 Pneumonia - Trial NCT06360770

Access comprehensive clinical trial information for NCT06360770 through Pure Global AI's free database. This phase not specified trial is sponsored by General and Teaching Hospital Celje and is currently Completed. The study focuses on Sepsis. Target enrollment is 35 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

Free Database
Powered by Pure Global AI
840K+ Trials
NCT06360770
Completed
Trial Details
ClinicalTrials.gov โ€ข NCT06360770
View on ClinicalTrials.gov
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Assessement of Microcirculation With NIRS Predicts Sepsis Development in Patients With Severe Covid-19 Pneumonia
Assessement of Microcirculation With NIRS Predicts Sepsis Development in Mechanically Ventilated Patients With Severe Covid-19 Pneumonia

Study Focus

Sepsis

Observational

Sponsor & Location

General and Teaching Hospital Celje

Celje, Slovenia

Timeline & Enrollment

N/A

Dec 01, 2021

Apr 30, 2023

35 participants

Primary Outcome

sepsis development

Summary

Sepsis and septic shock are among main causes of death in patients with severe Covid-19
 pneumonia. A few factors are proven to predict sepsis in these patients. WIth near infrared
 spectroscopy it is possible to detect microcirculatory changes typical for sepsis early in
 the course of disease. The hypothesis that changes in tissue oxygene saturation during
 vasoocclusive test predict sepsis as well as mortality in mechancally ventilated patients
 withe severe Covid-19 pneumonia will be tested.

ICD-10 Classifications

Other sepsis
Sepsis, unspecified
Other specified sepsis
Candidal sepsis
Puerperal sepsis

Data Source

ClinicalTrials.gov

NCT06360770

Non-Device Trial