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OpenTrials
Completed

NCT Number: NCT01186510

Lung Perfusion With Oxygenated Blood During Aortic Clamping

Pulmonary dysfunction presumably linked to an inflammatory response is frequent after cardiac operations using cardiopulmonary bypass (CPB) and pulmonary hypoperfusion.

Aim of the study: To evaluate the protective effect of continuous pulmonary perfusion with oxygenated blood during aortic crossclamping on the inflammatory response.

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Key information

Conditions

Postoperative Pulmonary Dysfunction

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Goethe University

Frankfurt am Main, 60590, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-80 ys
  • Cardiopulmonary bypass procedure
  • FEV1 <80%
  • COPD >II

Exclusion criteria

  • Emergency cases

Treatment and study plan

lung perfusion

Procedure

see literature of proceeding

no lung perfusion

Procedure

see literature of proceeding

Primary outcomes

  1. Inflammatory marker

    Time frame: 5 days

Sponsors and collaborators

Lead sponsor

Johann Wolfgang Goethe University Hospital

Other

Registry information

Acronym: PulPer-001-Sch

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Aug 23, 2010
Registry last updated
Jun 4, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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