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The effects of enoximone in acute exacerbation COPD: a pilot study

The effects of enoximone in acute exacerbation COPD: a pilot study - The effects of enoximone in acute exacerbation COPD: a pilot study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON49504
Enrollment
20
Registered
2020-01-15
Start date
2020-05-12
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute pulmonary attack Bronchospasm Exacerbation COPD

Interventions

Three doses of intravenous 0,5 mg/kg enoximone, leading to a total dose of 1.5 mg/kg enoximone

Sponsors

Rijnstate Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with an AE-COPD wherefore intubation occurred within 24 hours before enrollment.

Exclusion criteria

Exclusion criteria: Patients with known asthma or interstitial lung disease (ILD) Known neurodegenerative diseases such as Amyotrophic Lateral Sclerosis (ALS), Multiple Sclerosis (MS), Guillain-Barre and Dementia Hypertrophic obstructive cardiomyopathy (HOCM) Severe aortic stenosis with aortic valve area 1.5 Pregnancy

Design outcomes

Primary

MeasureTime frame
Auto-PEEP

Secondary

MeasureTime frame
Respiratory parameters: - Lungcompliance in L/cmH2O - Airway resistance in cmH2O/L/s - VCO2 - etCO2 - FiO2 Cardiac parameters: - RVSP - Cardiac output - TAPSE - MAPSE - Ejection Fraction of the Left Ventricle Arterial blood gas analysis (2 ml of blood, obtained through an arterial cannula): - pH, PaCO2, PaO2, saturation, lactate, base excess, Vital Signs: - Occurrence of adverse side effects such as (supraventricular) arrhythmics and hypotension

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)