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Clinical Trials/NCT01088074
NCT01088074
Completed
Not Applicable

A Comparative Study of Incision Closure Methods for Total Knee Arthroplasty

Foundation for Southwest Orthopedic Research1 site in 1 country75 target enrollmentJanuary 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Total Knee Replacement Closure
Sponsor
Foundation for Southwest Orthopedic Research
Enrollment
75
Locations
1
Primary Endpoint
Primary Outcome Measure
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The aim of the study is to compare incision closure techniques for total knee replacement using a combination of state-of-the-art sutures with tissue adhesives or staples in an effort to identify the best approach with respect to time efficiency, cost, durability, dehiscence, microbial resistance and cosmesis.

The hypothesis is that the combined suture/adhesive approach (sutures for capsule and subcutaneous layers, and tissue adhesive for the final cutaneous layer) or suture/staple approach will be significantly faster and of comparable durability as the conventional exclusive suture approach (sutures used for the capsule, subcutaneous, and cutaneous layers). This is a prospective, randomized, controlled, single site, unblinded (open label) study.

Registry
clinicaltrials.gov
Start Date
January 2009
End Date
October 2009
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Foundation for Southwest Orthopedic Research
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Inclusion criteria included 18 years or older
  • TKA scheduled without a bilateral planned within one week of the initial surgery
  • Willingness to attend prescribed physical therapy 3 times per week.

Exclusion Criteria

  • Exclusion criteria included medical conditions or personal circumstances that would prevent participation and completion of physical therapy and follow-up visits
  • Current participation in another clinical trial
  • Preoperative systemic infections
  • Uncontrolled diabetes, or diseases or conditions known to effect the wound healing process
  • Known hypersensitivity to cyanoacrylate
  • Formaldehyde, or the dye D\&C Violet #2
  • Prior knee hardware fixation devices
  • Prior knee incisions greater than 9cm, and arthrofibrosis as evidence by limited ROM less than 80°.

Outcomes

Primary Outcomes

Primary Outcome Measure

Time Frame: 1/2009-10/2009

The primary endpoint is the mean procedure time improvement for TKA incision closure using a combined suture/adhesive or suture/staple approach versus suture closure alone.

Secondary Outcomes

  • Mean postop hospital stay(1/2009-10/2009)

Study Sites (1)

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