Actively Recruiting

Phase 4
Age: 40Years +
All Genders
NCT05703919

Standard vs Targeted Oxygen Therapy Prehospital for Chronic Obstructive Pulmonary Disease

Led by Central Denmark Region · Updated on 2025-06-10

1888

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The STOP-COPD trial is a randomized, patient-blinded, prehospital clinical trial designed to evaluate the effect of titrated oxygen therapy compared to standard oxygen treatment in patients with suspected acute exacerbation of chronic obstructive pulmonary disease (AECOPD) treated with inhaled bronchodilators. The primary objective is to determine whether a titrated oxygen strategy targeting SpO₂ 88-92% can reduce 30-day mortality compared to the current standard practice using 100% compressed oxygen as a nebulizer driver.

CONDITIONS

Official Title

Standard vs Targeted Oxygen Therapy Prehospital for Chronic Obstructive Pulmonary Disease

Who Can Participate

Age: 40Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients over the age of 40
  • Suspected acute exacerbation of COPD by emergency medical personnel
  • Confirmed suspicion of COPD
Not Eligible

You will not qualify if you...

  • Bronchospasm caused by asthma, allergic reaction, or non-COPD conditions
  • Known or suspected pregnancy
  • Use of non-invasive, invasive, or assisted bag mask ventilation before enrollment
  • Allergy to inhaled bronchodilators such as Salbutamol
  • Inter-hospital transfer
  • More than 2 doses (5 mg each) of inhaled bronchodilator treatment given before study treatment
  • Suspicion of acute coronary syndrome

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Prehospital Emergency Medical Servises, Central Denmark Region

Aarhus N, Denmark, 8200

Actively Recruiting

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Research Team

M

Martin F Gude, PhD

CONTACT

A

Arne Sylvester R Jensen

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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