Value of Transthoracic Ultrasonography (TTU) for Etiological Diagnosis of Acute Dyspnea: Cross Sectional Study

Sponsor
Assiut University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05647655
Collaborator
(none)
143
15

Study Details

Study Description

Brief Summary

Evaluating the capability and efficiency of transthoracic ultrasound in attempting to identify the etiology of acute dyspnea.

Condition or Disease Intervention/Treatment Phase
  • Device: Ultrasonography

Detailed Description

Acute dyspnea is a frequent challenge for physicians due to having multiple etiologies, leading to difficulty in establishing an accurate diagnosis.

The presence of this symptom is already a predictor of increased mortality and a lot of investigations are required to differentiate between etiologies. Hence, prompt diagnosis is needed to streamline these patients' appropriate management and disposition from the ED.

Transthoracic ultrasound has traditionally been used for the detection of pleural effusion and evaluation of the chest wall, but the indications have been expanded.

The gold standard imaging technique for the majority of pulmonary disorders is high-resolution computed tomography (HRCT), but it has negatives which are:

  • hazard of ionizing radiation

  • high cost

  • being nonportable

Study Design

Study Type:
Observational
Anticipated Enrollment :
143 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Value of Transthoracic Ultrasonography (TTU) for Etiological Diagnosis of Acute Dyspnea: Cross Sectional Study
Anticipated Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Mar 1, 2024
Anticipated Study Completion Date :
Apr 1, 2024

Outcome Measures

Primary Outcome Measures

  1. Differentiate between different etiologies of acute dyspnea [Baseline]

    Analysis of ultrasound findings to differentiate between etiologies of acute dyspnea.

Secondary Outcome Measures

  1. Detect value of transthoracic ultrasound (TTU) in comparison to CT chest. [Baseline]

    Comparison between accuracy of TTU and CT

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Clinical history of acute dyspnea
Exclusion Criteria:
  • Subcutaneous emphysema.

  • Patients with more than 24 h interval between HRCT and TTU.

  • Patients with poor-quality of TTU image.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assiut University

Investigators

  • Principal Investigator: Ahmed A Elsayed, MBBCH, Assiut University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ahmed Alaa Eldin Abd El Moniem, Principal Investigator, Assiut University
ClinicalTrials.gov Identifier:
NCT05647655
Other Study ID Numbers:
  • US in Acute dyspnea
First Posted:
Dec 12, 2022
Last Update Posted:
Dec 16, 2022
Last Verified:
Dec 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 16, 2022