Effects of high-intensity noninvasive positive pressure ventilation on minute ventilation in stable hypercapnic COPD

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00000639

Enrollment

Registered

2011-01-17

Start date

2010-09-09

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

J96.1 J44.81

Interventions

Group 1: spontaneous breathing Group 2: ventilation with own ventilator Group 3: ventilation with Stellar 150, Resmed using original ventilator settings Group 4: ventilation with iVAPS mode

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: patients with chronic respiratory failure using noninvasive ventilation for more than 2 months

Exclusion criteria

Exclusion criteria: acute exazerbation (> 2 of the following signs: infiltrates in chest x-ray, increase of CRP or leukocytes, yellow or green sputum, fever

Design outcomes

Primary

Measure	Time frame
minute ventilation during different modes of ventilation measured with pneumotachograph	—

Secondary

Measure	Time frame
respiratory rate, ventilation pressure	—

Countries

Germany

Contacts

Public ContactEmelie Ekkernkamp

Universitätsklinik Freiburg, Abteilung Pneumologie

emelie.ekkernkamp@uniklinik-freiburg.de07612703706

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026