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NCT06233448 Clinical Trial

Thorathic Fluid Content as an Early Predictor of Weaning From Mechanical Ventilation in Acute Respiratory Distress Syndrome

Acute Respiratory Distress Syndrome Clinical Trial

Official title:
Thorathic Fluid Content as an Early Predictor of Weaning From Mechanical Ventilation in Acute Respiratory Distress Syndrome

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06233448
Other study ID # 36264PR504/1/24
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date February 2024
Est. completion date July 2024

Study information
Verified date January 2024
Source Tanta University
Contact Mei Abdallah
Phone 201008018208
Email Meikamal63@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Thorathic fluid content measurement using indirect cardiometry is required for prediction of Weaning from mechanical ventilation in cases of acute respiratory distress syndrome and its value in sucsess Weaning

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 50
Est. completion date July 2024
Est. primary completion date July 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - patients with ARDS on ventilator for more than 48 hr. proceed for extubation Exclusion Criteria: - heart, renal, hepatic failure Obesity , pregnancy Pneumothorax, pneumonia, hemorrhage

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Indirect cardiometry
Measurements of thorathic fluid content

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Tanta University

Outcome
Type Measure Description Time frame Safety issue
Primary Success of weaning from mechanical ventilation Number of participants without artificial aids for ventilation 48 hours
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