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Trials / Completed

CompletedNCT04442958

Effectiveness of Convalescent Immune Plasma Therapy

Effectiveness of Convalescent Immune Plasma Therapy in Severe COVID-19 Patients With Acute Respiratory Distress Syndrome

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Bagcilar Training and Research Hospital · Other Government
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

The aim of the study is to evaluate the safety, improvement of clinical symptoms and laboratory parameters of convalescent immune plasma treatment in severe Covid-19 patients with ARDS.

Detailed description

The aim of the study is to evaluate the safety, improvement of clinical symptoms with hypoxemia, metabolic and laboratory parameters of patients with convalescent immune plasma treatment in severe Covid-19 patients followed up in critical care unit.

Conditions

Interventions

TypeNameDescription
OTHERConvalescent Immune PlasmaOne dose of 200 mL of convalescent ımmune plasma derived from recently recovered donors with the neutralizing antibody titers above 1:640 was transfused to the patients as an addition to standart critical care treatment.

Timeline

Start date
2020-05-15
Primary completion
2020-06-15
Completion
2020-06-17
First posted
2020-06-23
Last updated
2020-07-01

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04442958. Inclusion in this directory is not an endorsement.

Effectiveness of Convalescent Immune Plasma Therapy (NCT04442958) · Clinical Trials Directory