Clinical impact of non invasive pressure support ventilation after extubation in major lung resectional surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00000311

Enrollment

Registered

2010-01-13

Start date

2005-04-22

Completion date

Unknown

Last updated

2025-10-06

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

Conditions

OPS 5-32: null J44

Interventions

Group 1: In the Control group ventilator support was given only to treat respiratory insufficiency. All patients (including arm 2) are receiving standard care included pain control, chest physiotherap

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Major lung resection (segmentectomy, lobectomy, bilobectomy, pneumonectomy) Predicted postoperative lung function (ppoFEV1) between 1,0 l * sec-1 und 1,5 l *sec-1 Maximal oxygen uptake VO2max greater than 10 ml * min-1 * kgKG-1

Exclusion criteria

Exclusion criteria: Severe congestive heart disease or coranary artery disease ppoFEV1: 2, respectively Withdrawal of patients consent

Design outcomes

Primary

Measure	Time frame
Reintubation and mortality rate in the first 30 days postoperative	—

Secondary

Measure	Time frame
Incidence of pneumonia and blood gas analyses intrahospital	—

Countries

Germany

Contacts

Public ContactWolfgang Körber

Ev. Krankenhaus Weende, Abt. Pulmologie, Beatmungsmedizin und Schlaflabor

koerber-goettingen@t-online.de0551-5034-2451

Outcome results

None listed

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