Impact of Different Perioperative Tourniquets on Blood Loss and Surgeon Satisfaction in Total Knee Arthroplasty

Recruiting N/A Interventional Study
Total Knee Arthroplasty
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
50 (estimated)
Sponsor
University Hospital, Bonn · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

The present study investigates the impact of two different perioperative tourniquets with different closing features on operative blood los, surgical field quality and surgeon satisfaction.

Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Inidication for a Total Knee Arthroplasty * Approval for Surgery by the Department of Anesthesia Exclusion Criteria: * Open Wounds of the lower extremities * Acute or chronic infections of the lower extremities
Contacts

Alexander Franz, Dr. med., B.Sc.

+49 170 3750718

alexander.franz@ukbonn.de

CONTACT