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Efficacy of convalescent plasma transfusion of COVID-19 survivors on the treatment of respiratory failure of these patients

Efficacy of convalescent plasma transfusion of COVID-19 survivors on the treatment of respiratory failure of these patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200406046968N2
Enrollment
30
Registered
2020-04-22
Start date
2020-05-04
Completion date
Unknown
Last updated
2020-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19 Disease. Coronavirus infection, unspecified site

Interventions

In 30 patients with respiratory failure and ARDS caused by COVID-19 undergoing mechanical ventilation or oxygen therapy, antivirals and supportive care therapies will be continued, and 200-400 cc of

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 years Confirmed COVID-19 clinically and positive PCR Severe bilateral pulmonary involvement on CT scan or chest x-ray Pao2/Fio2<300 Need for oxygen therapy or mechanical ventilation

Exclusion criteria

Exclusion criteria: Blood group incompatibility Pregnancy

Design outcomes

Primary

MeasureTime frame
Effect of convalescent plasma. Timepoint: Blood and plasma will be taken from patients who have been symptom free for 14-17 days. If it is less than 14 days, the donor should have 2 negative tests in two different days. Method of measurement: ELISA.

Secondary

MeasureTime frame
Oxygenation. Timepoint: Daily until discharge or death. Method of measurement: ABG.;SOFA score. Timepoint: Daily until discharge or death. Method of measurement: Questionnaire.;Duration of mechanical ventilation. Timepoint: until discharge or death. Method of measurement: Questionnaire.;Duration of admission. Timepoint: Daily until discharge or death. Method of measurement: Questionnaire.;Mortality. Timepoint: Admission period. Method of measurement: patient's file.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHaleh Mikaeili

Tabriz University of Medical Sciences

halehmikaeili@gmail.com+98 41 3329 6024

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026