Skip to content

Evaluation of the efficacy and safety of methylprednisolone pulse therapy in treatment of Covid-19 patients with Acute respiratory distress syndrome

Evaluation of the efficacy and safety of methylprednisolone pulse therapy in treatment of Covid-19 patients with ARDS

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200406046963N1
Enrollment
40
Registered
2020-04-22
Start date
2020-03-30
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. COVID-19

Interventions

Sponsors

Artesh University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patient with moderate to severe Covid-19 admitted to ICU PaO2/FiO2 Less than 300 Progression of disease severity and not responding to standard treatment prediction of intubation for next 24 hours

Exclusion criteria

Exclusion criteria: Uncontrolled diabetes mellitus Active GI bleeding history of corticosteroid hypersensitivity sever electrolyte imbalances Procalcitonin more than 0.5 active bacterial, viral ( HIV, Hepatitis) and fungal infection

Design outcomes

Primary

MeasureTime frame
Mortality rate. Timepoint: from including to study to 60 days. Method of measurement: observation.;Blood O2 saturation. Timepoint: before and during the study for 14 days. Method of measurement: pulse Oximeter.;Oxygen therapy need. Timepoint: before and during the study for 14 days. Method of measurement: Clinical.

Secondary

MeasureTime frame
Chest CT Scan changes 48 hours after starting pulse therapy. Timepoint: 48 hours after starting methylprednisolon pulse therapy. Method of measurement: Chest CT Scan.;ICU length of stay. Timepoint: During the study until ICU discharge. Method of measurement: Patients file.;Sequential Organ Failure Assessment (SOFA) Score changes. Timepoint: before and during the study. Method of measurement: clinical.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEbrahim Hazrati

Artesh University of Medical Sciences

dr.hazrart.e@gmail.com+98 21 8609 6350

Outcome results

None listed

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