Clinical Trials Logo
  1. Home
  2. Knee Arthroplasty
  3. NCT00367289
  4. Details
NCT00367289 Clinical Trial

CT for Diagnosis of Implant Stability in Revision Arthroplasty

Knee Arthroplasty Clinical Trial

Official title:
CT for Diagnosis of Implant Stability in Revision Arthroplasty

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00367289
Other study ID # ctosteolysis-HMO-CTIL
Secondary ID
Status Completed
Phase N/A
First received August 21, 2006
Last updated April 27, 2011
Start date October 2007
Est. completion date December 2008

Study information
Verified date August 2006
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

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.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients admitted for hip or knee revision arthroplasty

- age over 18

Exclusion Criteria:

- fractures

- dislocations

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Hadassah Medical Organization Jerusalem

Sponsors (1)
Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

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