COPD Trial, Recruiting NCT05671198 Sponsor: Isala Condition: COPD
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COPD Trial, Recruiting

NCT05671198
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are in hospital mainly because of a serious sudden worsening of COPD (Chronic Obstructive Pulmonary Disease).
  • You have been diagnosed with COPD according to recognised medical guidelines (GOLD 2018 definition).
  • A breathing test done within the last 5 years showed that your airways are significantly obstructed, meeting specific measurement thresholds (confirm with trial site).

Who may not be able to join:

  • Your blood is too acidic and has too much carbon dioxide at the time you arrive at hospital (confirm with trial site).
  • You need a breathing machine (either through a mask or a tube) for reasons other than COPD alone, such as very low oxygen levels, when you first arrive.
  • You have already been diagnosed with paralysis of the diaphragm (the main breathing muscle under your lungs).
  • It is not possible to take an ultrasound image of your diaphragm — for example, if you are on a ventilator or are unable to follow spoken instructions.
  • You are not able to give written consent, or you do not wish to take part.
  • You are pregnant.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 16 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Marieke Duiverman, M.D. PhD., University Medical Center Groningen

Phone: 00316463120231

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Isala
Registry
ClinicalTrials.gov
Start date
27 March 2023
Est. completion
1 March 2025

Where this trial is recruiting

🇳🇱 Netherlands

Primary endpoints

- To investigate the responsiveness of sonographic parameters to detect change in Borg score for dyspnea during hospitalisation for AECOPD without respiratory acidosis.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov