Quantification of recirculation during veno-venous extracorporeal membrane oxygenation (VV-ECMO) in severe respiratory insufficiency

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00005106

Enrollment

Registered

2013-06-25

Start date

2012-05-03

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

J80

Interventions

Group 1: The impact of recirculation, cardiac output and cannula position on oxygen delivery and arterial oxygen saturation as clinical endpoint should be daily assessed in patients with adult respira

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients which requires vv ECMO during ARDS and which gives written voluntary consent during ECMO

Exclusion criteria

Exclusion criteria: Unability to obtain written voluntary consent until end of vv ECMO

Design outcomes

Primary

Measure	Time frame
Arterial oxygen Saturation, Oxygen delivery, Recirculation fraction	—

Secondary

Measure	Time frame
Position of ECMO cannula, patient cardiac output	—

Countries

Germany

Contacts

Public ContactAndreas Böning

Klinik für Herz-, Kinderherz- und Gefäßchirurgie

Andreas.Böning@chiru.med.uni-giessen.de0641 985 44301

Outcome results

None listed

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