NCT04458480|Unknown
Loading search results
Sponsor study identifier
observational
60
1 country
1
Study Start
September 7, 2019
Actual (reported)Primary Completion
September 6, 2020
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Study Completion
March 6, 2021
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Rehabilitation is an important part of the post-operative treatment after TKA by consensus. This study intends to analysis whether fast inpatient rehabilitation after TKA can improve knee joint or general function, and ultimately explore for effects and values of fast inpatient rehabilitation after TKA.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
March 6, 2021
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Click on a node to explore related trials.
Some registry-reported names shown below are not yet linked in this graph.
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
September 7, 2019
Actual (reported)June 26, 2020
Actual (reported)July 7, 2020
Actual (reported)September 6, 2020
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
March 6, 2021
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
bilateral knee Rang Of Motion (ROM)
bilateral knee flexion and extension ROM are measured by articular protractor
1 day after TKA
bilateral quadriceps femurs
measured by manual muscle test (MMT)
1 day after TKA
hamstrings muscle strength
measured by manual muscle test (MMT)
1 day after TKA
Hospital for Special Surgery-Knee Rating scale (HSSKR)
to measure knee function, with the minimum 0 and maximum 100, higher score means a better outcome
1 day after TKA
Both exposed group and control group are undertaken TKA surgery and routine postoperative management for 2 days in orthopedics department. Exposed group patients are transferred from orthopedics department to rehabilitation department on 2nd day after TKA, and accept fast inpatient rehabilitation for 1 week before hospital discharge, while control group patients continue to accept routine peri-operative management and conventional oral instructions of exercises in orthopedics department until hospital discharge.
Both exposed group and control group are undertaken TKA surgery and routine postoperative management for 2 days in orthopedics department. Exposed group patients are transferred from orthopedics department to rehabilitation department on 2nd day after TKA, and accept fast inpatient rehabilitation for 1 week before hospital discharge, while control group patients continue to accept routine peri-operative management and conventional oral instructions of exercises in orthopedics department until hospital discharge.
Routine inpatient rehabilitation protocol, administered by licensed Physical Therapist, duration period of 1.5h-2h each time, 2 times for weekdays and 1 time for weekends, totally lasting for 1 week, are applied to the exposed group. After the fast inpatient rehabilitation for 1 week, the patients can get discharged if reaching to the rehabilitation goals of symptoms of pain and swell reduced, knee flexion ≥ 90° and knee extension ≥ 0°, quadriceps femurs and hamstrings muscle strength enhanced, recovery to aided standing and walking, and acquiring of rehabilitation training methods.
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
He/She is admitted to orthopedics department of Peking University Third Hospital and undertaken initial unilateral TKA due to osteoarthritis, rheumatoid arthritis, etc.
Peking University Third Hospital
Beijing, Beijing Municipality, 100191, China
Mouwang Zhou, MM
Peking University Third Hospital
First Submitted
June 26, 2020
First Posted
July 7, 2020
Study Start
September 7, 2019
Actual (reported)Primary Completion
September 6, 2020
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Adductor Canal Block and Multimodal Local Infiltration Analgesia in Patients Receiving Total Knee Arthroplasty
The Efficacy of Using CR and PS Prosthesis in Total Knee Replacement
modified Barthel Index (mBI)
to measure ADL, with the minimum 0 and maximum 100, higher score means a better outcome
1 day after TKA
Numerical Rating Scale (NRS) for pain
the minimum is 0 and maximum 10, higher score means a worse outcome
1 day after TKA
NRS for pain
6 weeks after TKA
NRS for pain
3 months after TKA
NRS for pain
6 months after TKA
Knee Injury and Osteoarthritis Outcome Score (KOOS)
to measure knee function and global function, with the minimum 0 and maximum 100, higher score means a better outcome
1 day after TKA
KOOS
6 weeks after TKA
KOOS
3 months after TKA
KOOS
6 months after TKA
Contact the study team to confirm eligibility.
Study Completion
March 6, 2021
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Last Updated
July 7, 2020
Record last verified: 2020-07
Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.
Source: ClinicalTrials.gov.
JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.
Source retrieved: