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This Study Compares Two Noninvasive Dynamic Tools: Lung Ultrasound and Transthoracic Echocardiography Using LVOT VTI. It Aims to Measure the Sensitivity and Specificity of LUS in Guiding Fluid Resuscitation and Early Detection of Fluid Responsiveness and to Prevent Volume Overload

ConditionsSeptic ShockFluid Reponsiveness
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAin Shams University

About this trial

Reliability of the LVOT-VTI versus lung ultrasonography for early detection of fluid intolerance during fluid resuscitation of septic patients.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adult patients aged ≥ 18 years with septic shock.

Mean arterial pressure (MAP) <65 mmHg.

Need fluid resuscitation.

Disqualifiers

Patient <18 years.

Refusal of patient or relative to participate in the study.

Other types of shock.

Morbid obesity.

Trial population

patient with septic shock applied by inclusion \& exclusion criteria .

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Early detection of fluid accumulation syndrome in septic shock patients using velocity time integral versus lung ultrasound

Time frame
12 hours
2

Early detection of fluid accumulation syndrome in septic shock patients using velocity time integral ursus lung ultrasound.

Time frame
12 hours

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ain Shams University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: