Title

Corticosteroid Reduction in COPD
The Effect of Reduced Corticosteroid Therapy in Patients With Acute Exacerbation of COPD
  • Phase

    Phase 4
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Intervention/Treatment

    prednisone ...
  • Study Participants

    318
This study explores whether patients hospitalized with chronic obstructive pulmonary disease (COPD) exacerbation may have fewer days with prednisolone and with the same treatment effect by controlling the treatment by daily measurements of eosinophils.
The most commonly used treatment for acute exacerbations of chronic obstructive pulmonary disease (AECOPD) is a 5-day treatment with corticosteroids in moderate-high dose. Some patients receive repeated treatments, although it has been shown that corticosteroids only have temporary beneficial effects and no effect in relation to serious incidents or mortality. It has been found that the higher accumulated prednisolone dose disables patients due to serious side effects, including pneumonia, dysregulated diabetes, bone fracture in the context of osteoporosis, mental disorder and adrenal insufficiency etc. However, the extent of the side effects is unknown. Recent research has shown that it is presumably only a small subset of COPD patients who benefit from corticosteroid therapy. This group can be identified by the biomarker "blood-eosinophils" as already measured on most AECOPD patients during hospitalization.

This is a randomized, controlled, multi-center, non-Inferiority trial evaluating the effect of eosinophil guided corticosteroid therapy to patients with AECOPD. The aim of the study is to investigate whether the accumulated dose corticosteroid treatment during admissions for AECOPD can be reduced, including the presumed side effects, while (still) remaining the optimal treatment effect.
Study Started
Aug 31
2016
Primary Completion
Sep 30
2018
Study Completion
Jan 31
2019
Last Update
Feb 08
2019

Blood eosinophil guided prednisolone treatment Experimental

Intravenous Solu-Medrol 80 mg, followed by prednisolone tablet 37.5 mg daily (maximum of 5 days in all) if the eosinophil count in the blood ≥ 0.3 x 10E9/L. Eosinophil count in the blood <0.3 x 10E9/L results in no treatment with prednisolone. If the patient is discharged during the treatment period, given treatment from the last measured eosinophil count the remaining days.

Standard of care Active Comparator

Intravenous Solu-Medrol 80 mg on the first day followed by 37.5 mg of prednisolone tablets (1 x 25 mg plus 1 x 12.5 mg) daily for 5 days

Criteria

Inclusion criteria:

Patients hospitalized with AECOPD
Age ≥ 40 years
Spirometry-verified COPD (defined as FEV1 / FVC ≤ 70%)
Chronic Obstructive Lung Disease (GOLD) class C or D
Inclusion within 24 hours after admission

Exclusion criteria:

Known with a diagnosis of asthma
Life expectancy less than 30 days
Serious exacerbation requiring invasive ventilation or admission to ICU
Allergy to systemic corticosteroids
Severe mental illness, which is not controlled by medication
People who are detained under the act on the use of coercion in psychiatry
Severe language problems or inability to provide written informed consent
Pregnancy and lactation
Systemic fungal infections
No Results Posted