Clinical Trials Directory

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

TypeNameDescription
DRUGMethylprednisolone (drug)ATC code: H02AB06. Can be changed to Prednisolone 50 mg orally.
DRUGHydrocortisoneATC-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.

Comparing Hydrocortisone and Prednisolone for Acute Exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD) (NCT06892210) · Clinical Trials Directory