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Effect of Methylprednisolone in treatment of COVID-19 patients

Evaluation of Methylprednisolone Administration as a Therapeutic Option in the Coronavirus disease 2019 (COVID-19): A Randomized Controlled Study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200204046369N1
Enrollment
82
Registered
2020-04-08
Start date
2020-08-07
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

the 2019 novel Corona virus (COVID-19). COVID-19 confirmed by laboratory testing.

Interventions

Intervention 1: Intervention group: In addition to the standard care recommended by the National Committee, an initial dose of 2mg/kg will be started for all patients in the case group. The patients w

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: RT-PCR documented SARS-CoV-2 carriage in a nasopharyngeal and oropharyngeal sample at admission Age over 18 years old O2 saturation of less than 92 in room air Hospitalized patients

Exclusion criteria

Exclusion criteria: A known contraindication to treatment with the steroid Breastfeeding and pregnant patients Uncontrolled diabetes mellitus Uncontrolled hypertension patients who had previously been treated with steroids for any reason O2 Saturation of above 92 in room air Dissatisfaction with the study enrollment Immunodeficiency disorders

Design outcomes

Primary

MeasureTime frame
The all-cause mortality in 28 days. Timepoint: 28 days. Method of measurement: Clinical follow-up.;Clinical status. Timepoint: 5 and 10 days after intervention. Method of measurement: 9-points WHO ordinal scale.

Secondary

MeasureTime frame
Intubation and need for ventilation, and also admission to ICU. Timepoint: 5 and 10 days after intervention. Method of measurement: Clinical follow-up.;Duration of hospital admission. Timepoint: 5 and 10 days after intervention. Method of measurement: Clinical follow-up.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohsen Moghadami

Shiraz University of Medical Sciences

moghadami@sums.ac.ir+98 71 3230 5410

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 15, 2026