Ventilution PMCF-Study

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00037744

Enrollment

Registered

2025-08-22

Start date

2025-09-25

Completion date

Unknown

Last updated

2026-06-01

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

Conditions

Invasive ventilation

Interventions

Group 1: Adult patients on invasive ventilation where the Ventilution System is applied for reduction of respiratory dead space

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Usage of Ventilution within intended use and by trained users written consent of patient or authorized representative

Exclusion criteria

Exclusion criteria: Applicability of contraindications for the use of Ventilution Missing written consent of patient or authorized representative

Design outcomes

Primary

Measure	Time frame
Technical robustness of the Ventilution System within the observation window -number of alarms (low/mid priority) per hour -number of user actions per hour	—

Secondary

Measure	Time frame
Effective reduction of dead space (in ml) by the Ventilution System	—

Countries

Germany

Contacts

Public ContactChristoph Gründler

Gründler GmbH

christoph.gruendler@gruendler.de+497441407610

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026