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Clinical Trials/NCT03240484
NCT03240484
Unknown
Not Applicable

Examining Effects of Spinal Arthrodesis on Outcomes Following Total Hip Arthroplasty

Ottawa Hospital Research Institute1 site in 1 country160 target enrollmentMay 15, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Spinal Fusion
Sponsor
Ottawa Hospital Research Institute
Enrollment
160
Locations
1
Primary Endpoint
Implant positioning
Last Updated
6 years ago

Overview

Brief Summary

The purpose of the study is to explore the long term functional status of people who have had both a spinal fusion procedure and a total hip replacement.

Detailed Description

The purpose of the study is to explore the long term functional status of people who have had both a spinal fusion procedure and a total hip replacement. Studies have found that those who have received spinal fusion may have worse outcomes following a total hip replacement than those who have not received a spinal fusion. The information obtained from this study will allow surgeons and researchers to better understand why some who've had a spine fusion have more complications post total hip replacement compared to those who did not have spinal fusion surgery.

Registry
clinicaltrials.gov
Start Date
May 15, 2017
End Date
June 1, 2021
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Wade Gofton

Orthopaedic Surgeon

Ottawa Hospital Research Institute

Eligibility Criteria

Inclusion Criteria

  • Willing to come to the Civic Campus for a surgical follow-up visit
  • Speaks English and/or French
  • Group 1 patients must have had a spine fusion (SF) and total hip arthroplasty (THA)
  • Group 2 patients must have had a total hip replacement (THA) and no history of spine fusion (SF)
  • Group 3 patients must have had a spine fusion (SF) and no history of total hip arthroplasty (THA)

Exclusion Criteria

  • Patient does not meet all 'inclusion' criteria
  • Patient is unable to answer questionnaires
  • Unable to get x-rays for other medical reasons
  • Severe dementia

Outcomes

Primary Outcomes

Implant positioning

Time Frame: 6months or greater post-operative

Radiographic assessment (x-ray cup orientation measurements)

Secondary Outcomes

  • Hip dysfunction and osteoarthritis outcome score (HOOS)(6months or greater post-operative)
  • SF-12 Questionnaire(6months or greater post-operative)
  • Oswestry low back disability questionnaire(6months or greater post-operative)
  • Oxford Hip Score(6months or greater post-operative)

Study Sites (1)

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