Skip to content

Comparing two medications (dexamethasone and methylprednisolone high dose) for the treatment of pneumonia in patients with COVID-19

Dexamethasone vs methylprednisolone high dose for COVID-19 pneumonia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN33037282
Enrollment
216
Registered
2020-11-27
Start date
2020-06-11
Completion date
Unknown
Last updated
2024-01-15

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

Conditions

COVID-19 (SARS-CoV-2 infection) related pneumonia Infections and Infestations

Interventions

From 11/06/2020, patients were treated with dexamethasone 6 mg QD for seven to 10 days if they required oxygen. After 15/09/2020, the clinic's protocol was modified to use methylpredn

Sponsors

Clínica Medellín - Grupo Quirónsalud
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Over 18 years of age 2. Hospitalized with COVID-19 pneumonia confirmed by positive Real-Time Reverse Transcription Polymerase Chain Reaction for SARS-CoV2 (RT-PCR SARS-CoV-2) by Berlin protocol 3. Radiological confirmation of pneumonia

Exclusion criteria

Exclusion criteria: 1. Contraindications associated with corticosteroids 2. Dissent for medical management 3. Death in the first 24 hours 4. Patient in palliative care or with a life expectancy of fewer than 6 months 5. If the patient required admission to the ICU and did not receive at least two doses of the corticosteroid 6. If the patient receives at least two doses of methylprednisolone but did not continue with prednisone, they were not included, but their outcome continued to be monitored 7. Patients who also received less than 2 days of dexamethasone treatment were withdrawn from study follow-up

Design outcomes

Primary

MeasureTime frame
Recovery time measured in days using patient records; recovery time determined as the time until hospital discharge when each of the following criteria were met: decrease in laboratory severity markers, improvement in symptoms, decrease in oxygen requirement until nasal cannula or supplementary oxygen removal, and at least two doses of the respective treatment have been received

Secondary

MeasureTime frame
Respiratory health measured using arterial blood gas results during the period of hospitalization (Cytokine Release Syndrome (CRS) defined as ventilatory impairment plus two of the following: C-reactive protein (CRP) greater than 10 mg/dl, serum ferritin greater than 1000 ng/ml, D-dimer greater than 900 ng/ml)

Countries

Colombia

Outcome results

None listed

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