Clinical Trials Directory

Trials / Completed

CompletedNCT00805051

Acquired Von Willebrand Syndrome in Severe Aortic Stenosis

Does an Acquired Von Willebrand Syndrome Influence Perioperative Blood Loss in Patients With Severe Aortic Stenosis Undergoing Aortic Valve Replacement?

Status
Completed
Phase
Study type
Observational
Enrollment
60 (actual)
Sponsor
University Hospital, Basel, Switzerland · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Patients with severe aortic stenosis often suffer from an acquired Von Willebrand syndrome by degeneration of the polymers during passage through the narrow valve leading to turbulences. We hypothesized that the diagnosis of acquired von Willebrand syndrome influence perioperative blood loss in patients undergoing open cardiac valve replacement.

Detailed description

Patients with severe aortic stenosis often suffer from an acquired Von Willebrand syndrome by degeneration of the polymers during passage through the narrow valve leading to turbulences. After written consent and an extended anamnesis of existing coagulopathy, we take three blood samples in these patients: before surgery, on the day after surgery and 4 weeks after surgery. We determine von Willebrand factor in lab and by a point-of-care platelet function analyzer (Multiplate TM). We measure amount of mediastinal drainage after 24 hours and blood product consumption in these patients.

Conditions

Timeline

Start date
2008-10-01
Primary completion
2010-05-01
Completion
2010-08-01
First posted
2008-12-09
Last updated
2011-09-30

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT00805051. Inclusion in this directory is not an endorsement.