Clinical Trials Logo

Clinical Trial Summary

All patients over 18 who undergo a revision of hip or knee arthroplasty will be included. Patients undergo a CT of the hip joint. A radiologist will mark the presence of cysts and bone loss and will assess implant stability.

After the surgery, the surgeon will fill a similar form.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT00367289
Study type Observational
Source Hadassah Medical Organization
Contact
Status Completed
Phase N/A
Start date October 2007
Completion date December 2008

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
Withdrawn NCT03421938 - Effect of Downhill-uphill Walking Exercises on Functional Level and Muscle Strength in Patients With Knee Arthroplasty.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
Completed NCT00803348 - Continuous Femoral Nerve Blockade and Readiness to Discharge Following Total Knee Arthroplasty N/A