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Reduction of Corticosteroid Use in Outpatient Treatment of Exacerbated COPD (RECUT)

Primary Purpose

Pulmonary Disease, Chronic Obstructive, Adverse Effect of Glucocorticoids and Synthetic Analogues, Disease Exacerbation

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Placebo
Prednisone
Sponsored by
Prof. Dr. Jörg Leuppi
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Disease, Chronic Obstructive focused on measuring Corticosteroid treatment, COPD, Primary Health Care, Randomized controlled trial

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Informed Consent as documented by signature
  • Age ≥40 years
  • History of ≥10 pack-years of smoking (past or present smokers)
  • Airway obstruction, defined as FEV1/FVC≤70%
  • Current acute exacerbation of COPD by clinical criteria, defined by the presence of at least two of the following:

    • Change of baseline dyspnea
    • Change of cough
    • Change of sputum quantity or purulence

Exclusion Criteria:

  • Diagnosis of asthma
  • Initial necessity of hospitalization
  • Women who are pregnant or breast feeding
  • Premenopausal women with insufficient contraception and anamnestic risk for pregnancy
  • Severe coexisting disease with life expectancy <6 months
  • Diagnosis of tuberculosis
  • Known severe immunosuppression or immunosuppression after solid organ or stem cell transplantation
  • Inability to follow study procedures, e.g. due to language problems, psychological disorders, dementia, etc. of the participant
  • Participation in another study involving an investigational drug
  • Previous enrolment into the current study

Sites / Locations

  • Kantonsspital BasellandRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Investigational treatment

Standard treatment

Arm Description

Patients included in the placebo group are receiving systemic corticosteroid treatment (equivalent of 40mg prednisone daily) for three days followed by two days of placebo.

Patients included in the control group are receiving systemic corticosteroid treatment (equivalent of 40mg prednisone daily) for five days as recommended in current guidelines.

Outcomes

Primary Outcome Measures

Time to next exacerbation

Secondary Outcome Measures

Cumulative glucocorticoid dose
Glucocorticoid side effects and complications
Change in FEV1
Hospitalization rate during index exacerbation
Overall mortality

Full Information

First Posted
February 11, 2015
Last Updated
September 5, 2023
Sponsor
Prof. Dr. Jörg Leuppi
Collaborators
Institut für Hausarztmedizin Basel, Kantonsspital Baselland Bruderholz
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1. Study Identification

Unique Protocol Identification Number
NCT02386735
Brief Title
Reduction of Corticosteroid Use in Outpatient Treatment of Exacerbated COPD
Acronym
RECUT
Official Title
Reduction of Corticosteroid Use in Outpatient Treatment of Exacerbated COPD - a Randomized, Double-blind, Non-inferiority Study (The "RECUT"-Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 2015 (undefined)
Primary Completion Date
September 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Prof. Dr. Jörg Leuppi
Collaborators
Institut für Hausarztmedizin Basel, Kantonsspital Baselland Bruderholz

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background Chronic obstructive pulmonary disease (COPD) is a major public health issue with no curative treatment. In Switzerland estimated 5-7% of the total population are suffering from this chronic disease. According to current guidelines corticosteroids are part of treatment of acute exacerbations in COPD patients. Several studies suggest that corticosteroids accelerate the recovery of forced expiratory volume in 1 second (FEV1), decrease duration of hospitalization, reduce treatment failure rate and improve clinical outcome. The additional therapeutic benefit on FEV1-recovery tough seems only to last for three to five days. The investigators recently published a hospital-based study showing that in patients presenting to emergency departments with acute exacerbation of COPD, a short five day treatment with systemic steroids was not inferior to a conventional 14 day treatment with regard to re-exacerbation. Cumulative corticosteroid dose could be reduced in this trial. To the investigators knowledge no data is available about the minimal necessary corticosteroid dose in an outpatient treatment setting so far. Aim The primary aim of this study is to investigate in an outpatient setting, whether a three day treatment with orally administered systemic corticosteroids is non-inferior to a five day treatment in acute exacerbation of COPD and if total glucocorticoid exposure can be reduced by shorter therapy. Hypothesis The investigators postulate, that in an outpatient setting, where generally less severe exacerbations are being treated, a three day treatment duration of systemic corticosteroids should be non-inferior to a five day treatment duration with regard to treatment benefits but decrease cumulative corticosteroid exposure. Design and Setting This study is going to be performed as a prospective, randomized, double-blind, placebo-controlled, non-inferiority trial in an outpatient setting. Randomization will be performed as block randomization with a 1:1 allocation. The investigators are going to recruit GPs in northwestern and central Switzerland. Methods The investigators are going to include patients presenting to GP's with acute exacerbation of COPD. When matching the investigators eligibility criteria and written informed consent is given, patients included in the study are receiving systemic corticosteroid treatment (equivalent of 40mg prednisone daily) for either five days (conventional arm) or three days (interventional arm) followed by two days of placebo for the interventional group. Pre-randomized, identically looking, numbered blisters are given to all patients included in the study. Antibiotic treatment (Amoxicillin/Clavulanic acid, 625mg 3/d, for ten days) is given to all patients with a CRP ≥50mg/l, COPD and known diagnosis of bronchiectasis, as well as patients presenting with all three of the following symptoms: change of baseline dyspnea, change of sputum quantity and sputum purulence. Further initial treatment and steroid treatment after inclusion is determined and documented by the GP. Patients will undergo follow-up visits at day three and seven by their GP as well as follow-up phone calls executed by the study center at day 30, 90 and 180.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Disease, Chronic Obstructive, Adverse Effect of Glucocorticoids and Synthetic Analogues, Disease Exacerbation
Keywords
Corticosteroid treatment, COPD, Primary Health Care, Randomized controlled trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
470 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Investigational treatment
Arm Type
Experimental
Arm Description
Patients included in the placebo group are receiving systemic corticosteroid treatment (equivalent of 40mg prednisone daily) for three days followed by two days of placebo.
Arm Title
Standard treatment
Arm Type
Active Comparator
Arm Description
Patients included in the control group are receiving systemic corticosteroid treatment (equivalent of 40mg prednisone daily) for five days as recommended in current guidelines.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Three days prednisone 40mg, two days placebo
Intervention Type
Drug
Intervention Name(s)
Prednisone
Intervention Description
Five days prednisone 40mg.
Primary Outcome Measure Information:
Title
Time to next exacerbation
Time Frame
Six month follow-up period after index exacerbation.
Secondary Outcome Measure Information:
Title
Cumulative glucocorticoid dose
Time Frame
Six month follow-up period after index exacerbation.
Title
Glucocorticoid side effects and complications
Time Frame
Six month follow-up period after index exacerbation.
Title
Change in FEV1
Time Frame
7 days follow-up period after index exacerbation.
Title
Hospitalization rate during index exacerbation
Time Frame
Six month follow-up period after index exacerbation.
Title
Overall mortality
Time Frame
Six month follow-up period after index exacerbation.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Informed Consent as documented by signature Age ≥40 years History of ≥10 pack-years of smoking (past or present smokers) Airway obstruction, defined as FEV1/FVC≤70% Current acute exacerbation of COPD by clinical criteria, defined by the presence of at least two of the following: Change of baseline dyspnea Change of cough Change of sputum quantity or purulence Exclusion Criteria: Diagnosis of asthma Initial necessity of hospitalization Women who are pregnant or breast feeding Premenopausal women with insufficient contraception and anamnestic risk for pregnancy Severe coexisting disease with life expectancy <6 months Diagnosis of tuberculosis Known severe immunosuppression or immunosuppression after solid organ or stem cell transplantation Inability to follow study procedures, e.g. due to language problems, psychological disorders, dementia, etc. of the participant Participation in another study involving an investigational drug Previous enrolment into the current study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joerg D. Leuppi, Prof.
Phone
+41 61 925 21 80
Email
joerg.leuppi@ksbl.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Andreas Zeller, Prof.
Email
andreas.zeller@ksbl.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joerg D. Leuppi, Prof.
Organizational Affiliation
Kantonsspital Basleland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kantonsspital Baselland
City
Liestal
State/Province
BL
ZIP/Postal Code
4410
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joerg Leuppi, Prof.
Phone
+41 61 925 21 80
Email
joerg.leuppi@ksbl.ch

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Links:
URL
http://www.goldcopd.org
Description
8. The Global Strategy for the Diagnosis, Management and Prevention of COPD, Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2014

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Reduction of Corticosteroid Use in Outpatient Treatment of Exacerbated COPD

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