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임상 레이더 AI
임상시험 NCT05744895은(는) 무릎 골관절염에 대해 진행중, 모집종료 상태입니다. 모든 세부 정보를 보려면 임상시험 레이더 카드 뷰와 AI 발견 도구를 확인하거나 여기에서 무엇이든 물어보세요.
하나의 임상시험이 필터 기준과 일치합니다.
카드 뷰

MAKO Total Knee Artroplasty

진행중, 모집종료
임상시험 세부 정보는 주로 영어로 제공됩니다. 하지만 임상 레이더 AI가 도와드릴 수 있습니다! '시험 설명하기'를 클릭하여 선택한 언어로 임상시험 정보를 확인하고, 이에 대해 AI와 논의해 보세요.
임상시험 NCT05744895은(는) 무릎 골관절염에 대해 알아보는 관찰연구입니다. 현재 상태는 진행중, 모집종료이며, 연구는 2021년 9월 14일에 시작되어 95명의 참여자를 모집하고 있습니다. 워싱턴 대학교 세인트루이스이(가) 진행하며, 2025년 6월 1일까지 완료될 예정입니다. ClinicalTrials.gov의 가장 최근 정보는 2025년 3월 25일에 갱신되었습니다.
간단한 개요
The purpose of this study is to determine the early clinical and radiographic outcomes of robotically assisted total knee arthroplasty with the MAKO surgical robot using the Triathlon knee system. Results of this study will be compared to those of a previously published cohort of patients from this institution who underwent TKA using non-robotic, manual instruments.

MAKO TKA patients will be given Fitbits and the Focus Motion Knee Brace to capture the data listed in attachment section. The results of this data will be compared to the control group to see if there is or there is not a difference in clinical outcomes with patients receiving Total knee surgery using the MAKO surgical robot versus those who got Total knee surgery without the MAKO robot.

상세한 설명
Research objectives:

The purpose of this study is to determine the early clinical and radiographic outcomes of robotically assisted total knee arthroplasty with the MAKO surgical robot using the Triathlon knee system. Mean weekly VAS pain score during the first 4 weeks is the primary end point. Results of this study will be compared to prospective cohort of patients in the IRB study 201805014 from this institution who underwent TKA using non-robotic, manual instruments

Primary Hypothesis: Patients receiving robotic TKA will have better early recovery, including lower mean weekly VAS pain score for the first 4 weeks postoperatively and higher functional outcome scores, than the manual TKA historical cohort.

Secondary Hypothesis:

Patients receiving robotic TKA will have more accurate component position and alignment than the manual TKA historical cohort.

Potential Contribution: This study would give us a better understanding of the clinical and radiographic outcomes of patients receiving robotic TKA versus manual TKA. It will identify potential advantages and disadvantages of robotic TKA using the MAKO surgical robot.

공식 제목

Early Outcomes of Total Knee Arthroplasty Using the MAKO Surgical Robot and Triathlon Knee

질환/상태
무릎 골관절염
기타 연구 식별자
  • 202106145
NCT 번호
실제 연구 시작일
2021-09-14
최신 업데이트 게시
2025-03-25
예상 연구 완료일
2025-06
계획된 등록 인원
95
연구종류
관찰연구
상태
진행중, 모집종료
시험군 / 개입
참가자 그룹/시험군개입/치료
Prospective Group- Robotic TKA Arm
Prospective TKA patient receiving total knee arthroplasty using the MAKO robotic machine
Device: Robotic MAKO Total Knee
Prospective TKA patient receiving total knee arthroplasty using the MAKO robotic machine
Focusmotion Knee Brace
Focusmotion knee brace measures range of motion during exercises
Fitbit Tracking Device
Fitbit will measure patients steps, HR, and sleep
Focusmotion APP
Will survey patients with PROMS
Control- manual total Knee arthroplasty
Patients who have had a manual total knee arthroplasty
해당 없음
주요결과변수
결과변수측정값 설명시간 범위
Early recovery
To determine if Robotic-arm assisted TKA (RA-TKA) allows for earlier recovery than manual TKA (MI-TKA). This will be measured by weekly VAS pain score. \[Time Frame: 1 day- post op\]
4 weeks
이차결과변수
결과변수측정값 설명시간 범위
Post op EOS measurements for alignment
To determine if Robotic-arm assisted TKA (RA-TKA) allows for more accurate component placement than manual TKA (MI-TKA). units of measurement will be inches.
1 year
적격성 기준

연령대
성인, 노인
최소 연령
18 Years
참여 가능한 성별
전체
  • Planning to undergo Unilateral primary total knee arthroplasty
  • 18 and up
  • Willing to sign informed consent
  • Willing to return for all follow-up visits
  • Smartphone or tablet device capable of running the Fitbit andFocusMotion platform

  • BMI > 45
  • Inflammatory arthritis
  • Narcotic use greater than 5 days per week
  • Walking aid for musculoskeletal or neurologic issue other than operative joint
  • Bilateral total knee arthroplasty
  • Patient with an active infection or suspected infection in the operative joint
  • The absolute and relative contraindications stated in the FDA cleared labeling for the device
Washington University School of Medicine logo워싱턴 대학교 세인트루이스476개의 진행 중인 임상시험 탐색 가능
Stryker Nordic logoStryker Nordic
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Missouri

Washington University School of Medicine, Creve Coeur, Missouri, 63141, United States