Influence of Closed Suction Drainage After Total Knee Replacement on Patient's Reported Outcome and Basic Morphology Results, and Inflammation Factors
| Registry | NCT03995160, acronym TKR |
|---|---|
| Status | Unknown |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: single, treatment |
| Enrollment | 100 (Estimated) |
| Sponsor | Medical University of Warsaw (Other); collaborators: Centre of Postgraduate Medical Education |
| Conditions | Total Knee Replacement |
| Interventions | Use of closed suction drainage following total knee arthroplasty, Abstain of using a closed suction drainage (Procedure) |
| Dates | start 2022-03-01 (estimated), primary completion 2022-11-02 (estimated), completion 2023-03-01 (estimated), first posted 2019-06-21, last updated 2021-10-06 |
Related Papers Related Patents Related Grants Related Experts
All trials for Total Knee Replacement All trials of Use of closed suction drainage following total knee arthroplasty All trials of Abstain of using a closed suction drainage
The aim of the study will be to compare functional outcomes, basic morphology results, number of blood transfusions, costs of hospitalization, and inflammation factors, following total knee replacement (with use of one type of endoprosthesis) comparing use of closed suction drainage (CSD). Use of closed suction drainage may have influence on patients functional outcome.
Patients with primary knee osteoarthritis will be included in a randomized controlled trial and assigned to total knee arthroplasty with or without closed suction drainage. Subjects will be evaluated preoperatively, 1-day, 3-, 6- and 12-month postoperatively.
Change in morphology results will be measured by comparing preoperative and postoperative levels of haematocrite, haemoglobin, erythrocytes, and platelets.
Change in the number of blood transfusions will be measured by analyzing the number of needed transfusion of packed red blood cells in the postoperative period during stay in the hospital.
Change in levels of inflammation factors will be measured by analyzing the level of C-reactive protein in first and third day postoperatively.
Change in body temperature wille be measured daily by analyzing body temperature from day of the surgery until the day of discharge from the hospital
Presence of haematoma will be evaluated daily in the postoperative period by clinical examination.
Change in Western Ontario and McMasters University Osteoarthritis Index (WOMAC) Pain Score will be measured from baseline (can be measured anytime to a maximum of one month before surgery) 3,6 and 12 months post-operatively
Change in Western Ontario and McMasters University Osteoarthritis Index (WOMAC) Function Score will be measured from baseline (can be measured anytime to a maximum of one month before surgery) 3,6 and 12 months post-operatively
Costs of hospitalization will be measured by comparing cost of hospitalization between two analyzed groups
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Total knee replacement with use of closed suction drainage | Active comparator | Procedure: Use of closed suction drainage following total knee arthroplasty | Use of closed suction drainage following total knee replacement in treatment of knee primary osteoarthritis |
| Total knee replacement without use of closed suction drainage | Active comparator | Procedure: Abstain of using a closed suction drainage | Without the use of closed suction drainage following total knee replacement in treatment of knee primary osteoarthritis |
Sex: All, ages: 50 Years to 80 Years
Inclusion Criteria: * patient's consent for anticipation in the study * arthroplasty in one knee Exclusion Criteria: * patient's lack of consent for anticipation in the study * haematological diseases * reoperations in the area of endoprosthesis * medical history of any surgical intervention on the lower limb