Clinical Trials Logo
  1. Home
  2. Knee Arthroplasty
  3. NCT01329081

Rehabilitation After Fast-track Total Knee Arthroplasty — HOLEST  

Knee Arthroplasty Clinical Trial

Official title:
Rehabilitation After Fast-track Total Knee Arthroplasty

Clinical Trial Summary

BACKGROUND In 2008 approximately 7,700 total knee arthroplasties (TKA) were performed in Denmark. The results after TKA is in general very good, the investigators have, however, discovered that patients following fast-track TKA still have a deficit 12 months postoperatively of 5-10% in health-related quality-of-life and 15-20% in activity and participation when compared to age- and gender matched population. A postoperative rehabilitation intervention has the potential to reduce or remove this observed deficit. The current evidence of postoperative rehabilitation after TKA is, however, scares and conflicting, and no studies have shown a lasting effect beyond 3 months postoperatively. PURPOSE The purpose of this study is to investigate if a 6-weeks postoperative rehabilitation intervention is more effective than supervised home training, and furthermore to investigate the cost-effectiveness of the intervention in a societal perspective. MATERIALS & METHODS The study is performed as a randomized clinical trial. In total 140 patients are included in the study. Inclusion criteria are age above 18 years, patients diagnosed as having knee arthrosis, patients receiving primary elective TKA, and patients who are able to and willing transport themselves to the rehabilitation center, which demands ability to walk 50 meter, and climb 10 stair steps. Exclusion criteria are unicompartmental or revision arthroplasty, any neurological disease, knee infection, and substantial pain or functional limitation hindering rehabilitation tested by physiotherapist prior to rehabilitation start. Primary endpoint is 6 months postoperatively and primary outcome measure is change in total score by using the knee specific questionnaire Oxford Knee Score.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01329081
Study type Interventional
Source University of Aarhus
Contact
Status Withdrawn
Phase N/A
View Details
See also
  Status Clinical Trial Phase
Recruiting NCT05279092 - Yale Steroid Enhanced Versus Exparel Nerveblock TKA RCT Study Phase 2
Completed NCT02581683 - Magnesium Sulfate in Adductor Canal Blocks Phase 4
Completed NCT02413996 - Effects of Virtual Reality Rehabilitation in Patients With Total Knee Arthroplasty N/A
Completed NCT01191593 - The Efficacy of Adductor-Canal-Blockade on Pain and Morphine Consumption After Revision Knee Arthroplasty Phase 4
Completed NCT01140815 - Functional Performance of the Journey Deuce Bicompartmental Versus the Genesis II Total Knee System Phase 4
Completed NCT03847324 - Physiotherapy and Therapeutic Education on Patients With Pain Catastrophism Scheduled for a Total Knee Arthroplasty N/A
Active, not recruiting NCT06096727 - The Energize! Study for Adults With Knee Replacement N/A
Active, not recruiting NCT01705886 - Clinical and Economic Comparison of Robot Assisted Versus Manual Knee Replacement
Terminated NCT01705366 - Clinical Outcomes of Knee Replacement
Recruiting NCT01225484 - Perioperative Analgesia After Knee Arthroplasty Phase 4
Completed NCT00367289 - CT for Diagnosis of Implant Stability in Revision Arthroplasty N/A
Withdrawn NCT03421938 - Effect of Downhill-uphill Walking Exercises on Functional Level and Muscle Strength in Patients With Knee Arthroplasty. N/A
Completed NCT04467970 - Unicompartmental Knee Arthroplasty vs High Tibial Osteotomy. N/A
Not yet recruiting NCT06130813 - Increased Perioperative Communication Program in Knee Arthroplasty N/A
Recruiting NCT06293144 - the 95% Effective Dose of Ciprofol for Adjunctive Sedation Undergoing Knee Arthroplasty in Elderly People Early Phase 1
Active, not recruiting NCT04679857 - Substitution of the PCL in TKA With UC or PS Design N/A
Completed NCT06293131 - Median Effective Dose of Ciprofol-Assisted Sedation for Elderly Patients Undergoing Knee Arthroplasty Early Phase 1
Completed NCT05091918 - Limited Market Release - MotionSense Clinical Use Evaluation N/A
Recruiting NCT02934802 - Non-Interventional Consecutive and Prospective Study of e.Motion® PS Pro Prosthesis in the Total Knee Artroplasty
Active, not recruiting NCT02791477 - Functional Results With Attune Fixed Bearing Posterior Stabilized Knee Arthroplasty (A-16) N/A