Influence of Closed Suction Drainage After Total Knee Replacement.

NCT03995160 — Not applicable, Unknown, 100 participants, Medical University of Warsaw

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Influence of Closed Suction Drainage After Total Knee Replacement on Patient's Reported Outcome and Basic Morphology Results, and Inflammation Factors

RegistryNCT03995160, acronym TKR
StatusUnknown
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: single, treatment
Enrollment100 (Estimated)
SponsorMedical University of Warsaw (Other); collaborators: Centre of Postgraduate Medical Education
ConditionsTotal Knee Replacement
InterventionsUse of closed suction drainage following total knee arthroplasty, Abstain of using a closed suction drainage (Procedure)
Datesstart 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

-Summary

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.

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+Detailed description

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

+Arms and interventions

ArmTypeInterventionsDescription
Total knee replacement with use of closed suction drainageActive comparatorProcedure: Use of closed suction drainage following total knee arthroplastyUse of closed suction drainage following total knee replacement in treatment of knee primary osteoarthritis
Total knee replacement without use of closed suction drainageActive comparatorProcedure: Abstain of using a closed suction drainageWithout the use of closed suction drainage following total knee replacement in treatment of knee primary osteoarthritis
  • Use of closed suction drainage following total knee arthroplasty (Procedure), also known as Redon's drain: Use of closed suction drainage following total knee arthroplasty
  • Abstain of using a closed suction drainage (Procedure): Abstain of using a closed suction drainage following total knee arthroplasty

+Outcome measures

Primary outcomes

  • Change in haematocrite levels [from baseline (can be measured anytime to a maximum of one month before surgery) to 1-day, 3,6 and 12 months post-operatively]: Measuring results of haematocrite (in percentage in 1 ml of blood sample)
  • Change in the number of blood transfusions [from baseline to the 1-,2-,3- days postoperatively]: Measuring the number of needed transfusion of packed red blood cells in the postoperative period
  • Change in levels of inflammation factors [from baseline (can be measured anytime to a maximum of one month before surgery) to 1-day, 3,6 and 12 months post-operatively]: Measuring the level of C-reactive protein
  • Change in haemoglobin levels [from baseline (can be measured anytime to a maximum of one month before surgery) to 1-day, 3,6 and 12 months post-operatively]: Measuring results of haemoglobin (g/dL)
  • Change in erythrocytes levels [from baseline (can be measured anytime to a maximum of one month before surgery) to 1-day, 3,6 and 12 months post-operatively]: Measuring results of erythrocytes (number/ml)
  • Change in platelets levels [from baseline (can be measured anytime to a maximum of one month before surgery) to 1-day, 3,6 and 12 months post-operatively]: Measuring results of platelets (number/ml)

Secondary outcomes

  • Change in Western Ontario and McMasters University Osteoarthritis Index (WOMAC) Pain Score from baseline [from baseline (can be measured anytime to a maximum of one month before surgery) 3,6 and 12 months post-operatively]: The WOMAC Pain score is derived from a sub-section of the Knee injury and Osteoarthritis Outcome Score (KOOS) Knee Survey. The WOMAC Pain scores range from 0-100 with lower scores considered lower pain.
  • Change in Western Ontario and McMasters University Osteoarthritis Index (WOMAC) Function Score from baseline [from baseline (can be measured anytime to a maximum of one month before surgery) 3,6 and 12 months post-operatively]: The WOMAC Function score is derived from a sub-section of the Knee injury and Osteoarthritis Outcome Score (KOOS) Knee Survey. The WOMAC Function scores range from 0-100 with lower scores considered to have better function.
  • Change in body temperature [from baseline to the 1-,2-,3- days postoperatively]: Measuring body temperature from day of the surgery to the hospital until the day of discharge from the hospital
  • Influence of using CSD on costs of hospitalization [from baseline to the one year postoperatively]: Comparing cost of hospitalization between two analyzed groups

+Eligibility

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

+Investigators