Recruiting NCT06947655
Impact of Different Perioperative Tourniquets on Blood Loss and Surgeon Satisfaction in Total Knee Arthroplasty
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: VBM Tourniquet, Adaptive Cuff.
- Who it may be relevant to
- Registry conditions: Total Knee Arthroplasty. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Germany
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Impact of Two Different Perioperative Tourniquets on Blood Loss, Surgical Field and Surgeon Satisfaction During Total Knee Arthroplasty
Overview
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.
Interventions
- Device VBM Tourniquet
Perioperative VBM-Tourniquet Application with a fixation pressure of 15mmHg. - Device Adaptive Cuff
Perioperative Delfi-Tourniquet Application with a fixation pressure of 15mmHg.
Primary outcome measures
- Blood Loss [Time frame: Perioperative]
- Surgeon Satisfaction [Time frame: Perioperative]
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Triple blind
- Primary purpose
- Other
Study locations
Germany · 1 center
- University Hospital Bonn — Bonn
Identifiers
NCT: NCT06947655 · 2024_J