TKA_Vanco: Infection Prevention After TKA With or Without Vancomycin

Sponsor
Centre of Postgraduate Medical Education (Other)
Overall Status
Recruiting
CT.gov ID
NCT05461651
Collaborator
(none)
1,800
1
2
88
20.5

Study Details

Study Description

Brief Summary

Prospective, Randomized, Double Blinded Trial Comparing Clinical, Radiological and Laboratory Outcomes in prevention of infection after Total Knee Arthroplasty With or Without Vancomycin.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Knee arthroplasty
N/A

Detailed Description

Infection after surgery is one of the most common complication after total knee replacement. Our prospective randomized study is intended to show if addition of vancomycin to the joint before the wound closure will decrease infection after operation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1800 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Prospective, Randomized, Double Blinded Trial Comparing Clinical, Radiological and Laboratory Outcomes in Prevention of Infection After Total Knee Arthroplasty With or Without Vancomycin.
Actual Study Start Date :
Sep 1, 2021
Anticipated Primary Completion Date :
Jan 1, 2028
Anticipated Study Completion Date :
Jan 1, 2029

Arms and Interventions

Arm Intervention/Treatment
Sham Comparator: Knee arthroplasty

Knee arthroplasty without addition of antibiotic wash oraz antibitiotic powder to the surgery site

Procedure: Knee arthroplasty
total or unilateral knee arthroplasty

Active Comparator: Knee arthroplasty + vancomycin

Knee arthroplasty with addition of vancomysin powder to the surgery site

Procedure: Knee arthroplasty
total or unilateral knee arthroplasty

Outcome Measures

Primary Outcome Measures

  1. Incidence of surgical site infection [up to 24 months]

    The incidence of deep and superficial SSI after knee arthroplasty

Secondary Outcome Measures

  1. Blood test - CRP [12 weeks,]

    inflammatory reaction - CRP

  2. Blood test - IL 6 [12 weeks,]

    inflammatory reaction - Il-6

  3. Functional tests [12 weeks,]

    hop-for-distance

  4. Functional tests [6 months,]

    hop-for-distance

  5. Functional tests [12 months]

    hop-for-distance

  6. Functional tests [24 months]

    hop-for-distance

  7. Knee injury and Osteoarthritis Outcome Score [6 weeks]

    Knee Injury and Osteoarthritis Outcome Score; KOOS is intended to be used for knee injury that can result in post traumatic osteoarthritis (OA); KOOS has high test-retest reliability. In patients with knee injury, ICCs for the Pain subscale range from 0.85-0.93, the Symptoms subscale from 0.83-0.95, the ADL subscale from 0.75-0.91, the Sport/Rec subscale from 0.61-0.89 and the QOL subscale from 0.83-0.95. In patients with knee OA, ICCs for the Pain subscale range from 0.8-0.97, the Symptoms subscale from 0.74-0.94, the ADL subscale from 0.84-0.94, the Sport/Rec subscale from 0.65-0.92 and the QOL subscale from 0.6-0.91 (4).

  8. Knee injury and Osteoarthritis Outcome Score [6 months]

    Knee Injury and Osteoarthritis Outcome Score; KOOS is intended to be used for knee injury that can result in post traumatic osteoarthritis (OA); KOOS has high test-retest reliability. In patients with knee injury, ICCs for the Pain subscale range from 0.85-0.93, the Symptoms subscale from 0.83-0.95, the ADL subscale from 0.75-0.91, the Sport/Rec subscale from 0.61-0.89 and the QOL subscale from 0.83-0.95. In patients with knee OA, ICCs for the Pain subscale range from 0.8-0.97, the Symptoms subscale from 0.74-0.94, the ADL subscale from 0.84-0.94, the Sport/Rec subscale from 0.65-0.92 and the QOL subscale from 0.6-0.91 (4).

  9. Knee injury and Osteoarthritis Outcome Score [12 months]

    Knee Injury and Osteoarthritis Outcome Score; KOOS is intended to be used for knee injury that can result in post traumatic osteoarthritis (OA); KOOS has high test-retest reliability. In patients with knee injury, ICCs for the Pain subscale range from 0.85-0.93, the Symptoms subscale from 0.83-0.95, the ADL subscale from 0.75-0.91, the Sport/Rec subscale from 0.61-0.89 and the QOL subscale from 0.83-0.95. In patients with knee OA, ICCs for the Pain subscale range from 0.8-0.97, the Symptoms subscale from 0.74-0.94, the ADL subscale from 0.84-0.94, the Sport/Rec subscale from 0.65-0.92 and the QOL subscale from 0.6-0.91 (4).

  10. Knee injury and Osteoarthritis Outcome Score [24 months]

    Knee Injury and Osteoarthritis Outcome Score; KOOS is intended to be used for knee injury that can result in post traumatic osteoarthritis (OA); KOOS has high test-retest reliability. In patients with knee injury, ICCs for the Pain subscale range from 0.85-0.93, the Symptoms subscale from 0.83-0.95, the ADL subscale from 0.75-0.91, the Sport/Rec subscale from 0.61-0.89 and the QOL subscale from 0.83-0.95. In patients with knee OA, ICCs for the Pain subscale range from 0.8-0.97, the Symptoms subscale from 0.74-0.94, the ADL subscale from 0.84-0.94, the Sport/Rec subscale from 0.65-0.92 and the QOL subscale from 0.6-0.91 (4).

  11. 36-Item Short Form Survey [6 weeks]

    Quality of life, pain SF-36

  12. 36-Item Short Form Survey [6 months]

    Quality of life, pain SF-36

  13. 36-Item Short Form Survey [12 months]

    Quality of life, pain SF-36

  14. 36-Item Short Form Survey [24 months]

    Quality of life, pain SF-36

  15. Visual analog Scale [6 weeks]

    Pain Visual Analog Scale The pain VAS is a unidimensional measure of pain intensity. The most simple VAS is a straight horizontal line of fixed length, usually 100 mm. The ends are defined as the extreme limits of the parameter to be measured (symptom, pain, health)[8] orientated from the left (worst) to the right (best).

  16. Visual analog Scale [6 months]

    Pain Visual Analog Scale The pain VAS is a unidimensional measure of pain intensity. The most simple VAS is a straight horizontal line of fixed length, usually 100 mm. The ends are defined as the extreme limits of the parameter to be measured (symptom, pain, health)[8] orientated from the left (worst) to the right (best).

  17. Visual analog Scale [12 months]

    Pain Visual Analog Scale The pain VAS is a unidimensional measure of pain intensity. The most simple VAS is a straight horizontal line of fixed length, usually 100 mm. The ends are defined as the extreme limits of the parameter to be measured (symptom, pain, health)[8] orientated from the left (worst) to the right (best).

  18. Visual analog Scale [24 months]

    Pain Visual Analog Scale The pain VAS is a unidimensional measure of pain intensity. The most simple VAS is a straight horizontal line of fixed length, usually 100 mm. The ends are defined as the extreme limits of the parameter to be measured (symptom, pain, health)[8] orientated from the left (worst) to the right (best).

  19. Tegner Lysholm Knee Scoring Scale [6 weeks]

    The Lysholm Knee Scoring Scale is a patient-reported instrument that consists of subscales for pain, instability, locking, swelling, limp, stair climbing, squatting, and the need for support. Scores range from 0 (worse disability) to 100 (less disability).

  20. Tegner Lysholm Knee Scoring Scale [6 months]

    The Lysholm Knee Scoring Scale is a patient-reported instrument that consists of subscales for pain, instability, locking, swelling, limp, stair climbing, squatting, and the need for support. Scores range from 0 (worse disability) to 100 (less disability).

  21. Tegner Lysholm Knee Scoring Scale [12 months]

    The Lysholm Knee Scoring Scale is a patient-reported instrument that consists of subscales for pain, instability, locking, swelling, limp, stair climbing, squatting, and the need for support. Scores range from 0 (worse disability) to 100 (less disability).

  22. Tegner Lysholm Knee Scoring Scale [24 months]

    The Lysholm Knee Scoring Scale is a patient-reported instrument that consists of subscales for pain, instability, locking, swelling, limp, stair climbing, squatting, and the need for support. Scores range from 0 (worse disability) to 100 (less disability).

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Gosnartrosis
Exclusion Criteria:
  • no informed consent to participate in the study age under 40 multilligament injury or single plane knee instability another musculoskeletal disorders in lower limb ASA score > II

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Orthopaedics and Traumatology, Postgraduate Center for Medical Education, Professor A. Gruca Teaching Hospital Otwock Mazowieckie Poland 05-400

Sponsors and Collaborators

  • Centre of Postgraduate Medical Education

Investigators

  • Study Chair: Rafal KAminski, CMKP

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rafał Kamiński, Professor, Centre of Postgraduate Medical Education
ClinicalTrials.gov Identifier:
NCT05461651
Other Study ID Numbers:
  • TKA
First Posted:
Jul 18, 2022
Last Update Posted:
Jul 18, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Rafał Kamiński, Professor, Centre of Postgraduate Medical Education
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 18, 2022