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Clinical Trials/NCT07836608
NCT07836608Not yet recruitingNot Applicable

Is Use of the Watson Extraction System Associated With Reduced Operative Time and Safer Stem Extraction? - A Randomized Controlled Trial

Ottawa Hospital Research Institute1 site in 1 country20 target enrollmentStarted: October 1, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
20
Locations
1
Primary Endpoint
Timing of surgery

Study Overview

Brief Summary

A revision total hip replacement surgery requires the surgeon to remove, or extract, the femoral stem (the rod that was placed into the thigh bone during your first hip replacement). A variety of tools and techniques can be used to do this. At The Ottawa Hospital (TOH) surgeons attempt to remove the stem using less invasive measures, such as osteotomes, a tool that separates the stem from the bone, but if it doesn't work, they may need to perform an extended trochanteric osteotomy (ETO). An ETO is more invasive and increases the risk of complications.

The Watson Extraction System (WES) is another Health Canada approved tool that goes around the stem to help remove the femoral stem from the thigh bone. Research shows that the WES has been studied in case series of a few people, and the results seem promising, reducing the time of extraction and need for ETO. However, it is not clear if it offers better results than what is currently done at TOH.

The purpose of this study is to compare the WES to the current/usual care care at TOH to determine whether the WES can remove the femoral stem more efficiently (in less time and at a lower hospital cost) and effectively, while improving patient safety.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Over 18 years of age
  • •Undergoing revision Total Hip Arthroplasty for septic or aseptic indications
  • •Have well-fixed femoral components, of blade-stem design (collared and collarless)

Exclusion Criteria

  • •Tapered stem in situ less than 4 months
  • •Cemented Stems
  • •Femoral Stems with Trunnions > 14mm
  • •Femoral Stems of alternative design not compatible for use with the WES

Arms & Interventions

Watson Extraction System (WES)

Experimental

Participants randomized to this arm will undergo stem extraction utilizing the WES in addition to other standard of care equipment, as required. Surgeons will use the WES device for extraction first.

Intervention: Watson Extraction System (Device)

Current Standard of Care at TOH

Active Comparator

Participants randomized to this arm will undergo stem extraction as per surgeon preference with the use of K-wires, burr and flexible osteotomes. An ETO will be performed as per surgical judgement.

Intervention: Standard of Care Stem Extraction (Procedure)

Outcomes

Primary Outcomes

Timing of surgery

Time Frame: From surgery start to surgery close

The time it take to complete the surgery, including the femoral stem extraction

Time of Femoral Stem Extraction

Time Frame: From start of femoral stem extraction to end of femoral stem extraction, up to 60 minutes

Amount of time, in minutes, it takes to remove the femoral stem during surgery

Secondary Outcomes

  • Intraoperative complication rate(From surgery start to surgery close)
  • Postoperative Complication Rate(From end of surgery to 3 months postoperative)
  • Change in Patient Reported Outcomes from baseline to 3 months(Baseline and at 3 month following surgery)
  • Cost of OR time and resources(From start of surgery to end of surgery)
  • Cost of complications(From end of surgery to 3 months postoperative)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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