High Volume Specialty Knee Replacement Surgeons Achieve Better Clinical and Quality-of-Life Scores

Sponsor
Singapore General Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT00999570
Collaborator
(none)
3,458
1
47
73.6

Study Details

Study Description

Brief Summary

To determine whether specialty training or high volume of operative experience is associated with better clinical outcome and quality-of-life scores.

Condition or Disease Intervention/Treatment Phase
  • Other: Specialty training for knee surgeons

Detailed Description

Primary total knee replacements are becoming a commonly performed procedure. Many general orthopaedists can perform large numbers of such surgeries. Thus, we aim to find out if there is value of having surgeons with AR fellowship training to perform primary total knee arthroplasty. This has an implication in the direction of the training of future AR surgeons and in the distribution of operative cases.

Study Design

Study Type:
Observational
Actual Enrollment :
3458 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
High Volume Specialty Knee Replacement Surgeons Achieve Better Clinical and Quality-of-Life Scores
Study Start Date :
Jan 1, 2004
Actual Primary Completion Date :
May 1, 2007
Actual Study Completion Date :
Dec 1, 2007

Arms and Interventions

Arm Intervention/Treatment
Patients operated by AR trained surgeons

patients who had their total knee replacements performed by surgeons who have completed a fellowship training in adult reconstruction surgery

Other: Specialty training for knee surgeons

Patients operated by non-AR surgeons

patients who had their total knee replacements performed by orthopaedic surgeons who did not complete an adult reconstruction fellowship training

Outcome Measures

Primary Outcome Measures

  1. To determine whether specialty training or high volume of operative experience is associated with better clinical outcome and quality-of-life scores. [2 years]

Secondary Outcome Measures

  1. To determine which other factors are predictors of better outcome score and quality-of-life scores. [2 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
37 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients who require total knee arthroplasty seen during the specified period
Exclusion Criteria:
  • revision total knee arthroplasty

  • unicompartmental or bicompartmental knee arthroplasty

Contacts and Locations

Locations

Site City State Country Postal Code
1 Singapore General Hospital Singapore Singapore 169608

Sponsors and Collaborators

  • Singapore General Hospital

Investigators

  • Principal Investigator: Sok Chuen Tan, MBBS, MRCS, Singapore General Hospital
  • Study Director: Seng Jin Yeo, FRCS, FAMS, Singapore General Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00999570
Other Study ID Numbers:
  • 2009/626/D
First Posted:
Oct 22, 2009
Last Update Posted:
Oct 22, 2009
Last Verified:
Oct 1, 2009

Study Results

No Results Posted as of Oct 22, 2009