NCT06947655 Impact of Different Perioperative Tourniquets on Blood Loss and Surgeon Satisfaction in Total Knee Arthroplasty
| NCT ID | NCT06947655 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University Hospital, Bonn |
| Condition | Total Knee Arthroplasty |
| Study Type | INTERVENTIONAL |
| Enrollment | 50 participants |
| Start Date | 2024-10-01 |
| Primary Completion | 2025-12-31 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 50 participants in total. It began in 2024-10-01 with a primary completion date of 2025-12-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief 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 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
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06947655 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Total Knee Arthroplasty. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06947655 currently recruiting?
Yes, NCT06947655 is actively recruiting participants. Contact the research team at alexander.franz@ukbonn.de for enrollment information.
Where is the NCT06947655 trial being conducted?
This trial is being conducted at Bonn, Germany.
Who is sponsoring the NCT06947655 clinical trial?
NCT06947655 is sponsored by University Hospital, Bonn. The trial plans to enroll 50 participants.