Clinical Trials Directory

Trials / Completed

CompletedNCT04922814

Comparison for the Effect of Neuromuscular Blocking Agents Versus Sedation Alone on Severe ARDS Patients Due to COVID-19

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Assiut University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Many questions about management of COVID-19 are still not answered. So, we recruit this study aiming to evaluate improvement of oxygenation in COVID-19 patients with severe ARDS, to improve morbidity and mortality of ICU covid patients, to participate in understanding of real hidden pathophysiology of COVID-19.

Conditions

Interventions

TypeNameDescription
DRUGmuscle relaxationThey will receive muscle relaxation treatment for at least 48 hours. Cisatracurium will be given. Short term infusions up to 24 hours will be given in a dose rate of 2-3 mic/Kg/min followed by intervallic shots of 2-5 mg.

Timeline

Start date
2021-08-01
Primary completion
2022-03-01
Completion
2022-08-01
First posted
2021-06-11
Last updated
2025-12-24

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04922814. Inclusion in this directory is not an endorsement.