M17
Conditions
Interventions
Group 1: Patients who underwent primary total knee arthroplasty between 2019 and 2021 under the administration of tranexamic acid
Sponsors
Orthopädische Klinik König-Ludwig-Haus
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Primary total knee arthroplasty under the use of tranexamic acid
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Estimated perioperative blood loss using pre- and postoperative lab values | — |
Secondary
| Measure | Time frame |
|---|---|
| Acute postoperative pain intensity (numeric rating scale 0-10) and mobility (range of motion, walking skills) assessed by the hospital's physiotherapists who were completely blinded to the application regime of tranexamic acid. Long-term follow up by PROMS (WOMAC-Score) after 3 and 12 months. | — |
Countries
Germany
Contacts
Public ContactAxel Jakuscheit
Orthopädische Klinik König-Ludwig-Haus
Outcome results
None listed