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Clinical Trials in Germany / NCT06947655
Recruiting Not applicable

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

NCT06947655 · tracked via the Priya Life Science Germany tracker
Sponsor
University Hospital, Bonn
Phase
Not applicable
Started
2024-10-01
Last updated
2025-04-27

Condition(s) studied

Total Knee Arthroplasty

Investigational drug(s) / intervention(s)

VBM TourniquetAdaptive Cuff

VBM Tourniquet: Perioperative VBM-Tourniquet Application with a fixation pressure of 15mmHg.

Adaptive Cuff: Perioperative Delfi-Tourniquet Application with a fixation pressure of 15mmHg.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Hospital Bonn Bonn North Rhine-Westphalia Recruiting

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Other trials for the same condition

Return to Activity After Total Knee Arthroplasty Enrolling by invitation
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06947655 on ClinicalTrials.gov ↗ ← All trials in Germany