Actively Recruiting

Age: 22Years - 80Years
All Genders
ID06971042

Early Diagnosis of Acute Respiratory Distress Syndrome (ARDS) in Mechanically Ventilated Patients Using Lung Ultrasound Score Compared to CT Chest

Led by Tanta University · Updated on 2025-06-29

20

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the use of lung ultrasound scores to diagnose acute respiratory distress syndrome (ARDS) early in patients expected to require mechanical ventilation for more than 24 hours. ARDS is a serious lung condition with poor oxygen levels and lung damage, often seen in critically ill patients. This study compares lung ultrasound, a bedside, radiation-free tool, to computed tomography (CT) scans, the current gold standard for diagnosing ARDS, to evaluate its accuracy and usefulness. The study involves examining patients using lung ultrasound with a portable machine while they lie on their backs. This noninvasive technique is quick, safe, and does not expose patients to radiation. The research aims to see if lung ultrasound can effectively identify ARDS and assess its severity within 48 hours, compared to CT chest scans that require moving the patient to a specialized unit. Participants will be monitored closely during the study, with lung ultrasound and CT scans performed to evaluate lung conditions. Researchers will measure how accurately lung ultrasound detects ARDS and its severity early on. The study will collect data within 48 hours of mechanical ventilation initiation, focusing on diagnosis and severity assessment. This observational study does not involve experimental treatments but focuses on improving diagnostic methods in critical care settings.

CONDITIONS

Brief Title

Early Diagnosis of ARDS in Mechanically Ventilated Patient Using LUS Score in Comparison With CT

Who Can Participate

Age: 22Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged more than 21 years old of both sexes
  • Patients expected to be mechanically ventilated for more than 24 hours
  • Patients suspected to have acute respiratory distress syndrome according to Berlin definition, starting within 1 week of a known insult such as trauma with lung contusions
Not Eligible

You will not qualify if you...

  • Patient's first guardian refuses inclusion in the study
  • History of pre-existing lung disease such as tumors or interstitial lung diseases
  • Cases of volume overload
  • Patients with acute kidney injury or renal failure

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Within 48 hours

Participants undergo lung ultrasound examinations and lung computed tomography scans to diagnose acute respiratory distress syndrome (ARDS) and assess its severity.

1 to 2 visits depending on diagnostic procedures

Long-term Monitoring

Duration - Up to study completion

Participants are observed for longer-term outcomes related to ARDS after initial diagnostic assessments.

Visits as needed during follow-up period

Trial Site Locations

Total: 1 location

1

Tanta university

Tanta, Egypt, 31527

Actively Recruiting

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Research Team

R

Roaa Elshamy, MSc

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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