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Fluid Responseveness in Sepsis and Its Correlation to CVP

NCT05612529 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 45

Last updated 2023-01-30

No results posted yet for this study

Summary

Introduction Aim of the work Patients and methods Type of study Exclusion criteria Statistical analysis Research ethics Reference

Conditions

  • Septic Shock

Interventions

DEVICE

US , Echocardiography

* Carotid ultrasonography: Parameters will be measured by single blinded independent examiner using an ultrasound device. Baseline carotid FTc, ΔVpeak, will be measured. * Echocardiography: Stroke Volume will be measured by transthoracic echocardiography. * Renal and splenic Doppler resistivity index. * Inferior vena cava collapsibility and distensibility indices. * Central venous pressure estimation by central venous catheter, and central - Lung ultrasound for detection of lung congestion * Lung ultrasound for detection of lung congestion.

Sponsors & Collaborators

  • Assiut University

    lead OTHER

Principal Investigators

  • olfat M elshinawy, professor · Assiut University

  • mohamed M abdelhady, professor · Assiut University

  • arafa M aboelhassan · Assiut University

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-01
Primary Completion
2022-11-30
Completion
2022-11-30

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05612529 on ClinicalTrials.gov