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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04463303
Other study ID # LULTRASOUND
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 2020
Est. completion date July 2021

Study information

Verified date July 2020
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the work is to

1. Assess the incidence of weaning induced pulmonary adema(WIPO).

2. Assess the risk factors of WIPO.

3. Evaluate the role of lung ultrasound in detecting WIPO during spontenous breathing trial(SBT).

4. Detect the threshold of B-line increase (Delta-B-lines) that provided the best diagnostic accuracy of WIPO.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date July 2021
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group N/A to 60 Years
Eligibility Inclusion Criteria:

- The study will include patients on mechanical ventilation who will be suitable for spontaneous breathing trial (SBT).

Exclusion Criteria:

- Patients with poor lung ultrasound window, history of cardiomyopathy, significant valvular disease (aortic or mitral insufficiency of grade = 2, mild or severe aortic and mitral stenosis) will be excluded from the study.

Study Design


Related Conditions & MeSH terms

  • Detecting the Number of B-lines in Lung Ultrasound and Its Accuracy in Diagnosis of Weaning Induced Pulmonary Oedema
  • Edema
  • Pulmonary Edema

Intervention

Other:
lung ultrasound
patient with or without weaning induced pulmonary adema

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary the number of B-lines in lung ultrasound and its accuracy in diagnosis of weaning induced pulmonary oedema 1 year