Trials / Recruiting
RecruitingNCT06892210
Comparing Hydrocortisone and Prednisolone for Acute Exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD)
- Status
- Recruiting
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 2,000 (estimated)
- Sponsor
- Copenhagen Respiratory Research · Network
- Sex
- All
- Age
- 40 Years
- Healthy volunteers
- Not accepted
Summary
The goal of this cluster randomized controlled trial is to determine the optimal treatment for Acute Exacerbation of Chronic Obstructive Pulmonary Disease. The study compares the effects and side effects of hydrocortisone and prednisolone in patients above 40 years old diagnosed with chronic obstructive pulmonary disease with acute exacerbation. The main question is whether there is a difference in readmission for COPD excerbation or all cause mortality within thirty days. Participants will randomized to receive treatment with either hydrocortisone or prednisolone.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Methylprednisolone (drug) | ATC code: H02AB06. Can be changed to Prednisolone 50 mg orally. |
| DRUG | Hydrocortisone | ATC-code: H02AB09. Can be changed to 50 mg x 4 daily orally if appropriate. |
Timeline
- Start date
- 2026-03-10
- Primary completion
- 2030-08-01
- Completion
- 2030-11-01
- First posted
- 2025-03-24
- Last updated
- 2026-03-18
Locations
14 sites across 1 country: Denmark
Source: ClinicalTrials.gov record NCT06892210. Inclusion in this directory is not an endorsement.