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CompletedNCT01320371Updated Feb 4, 2014

Analysis of Standard Versus Barbed Sutures in Primary Total Knee Arthroplasty.

An observational study in Arthropathy of Knee, sponsored by University of Utah. Completed at 4 sites in United States. Open to participants aged 18 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2014-02-04.

Sponsored by University of Utah · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
363
Ages
18 Years to 80 Years
Sex
All
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Study summary

The purpose of this prospective study is determine if barbed sutures are more efficient, have comparable complication rates, clinical outcomes, and cosmesis outcomes versus traditional knotted sutures when used in the closure of primary total knee arthroplasty (TKA).

Barbed suture has been associated with improved closure efficiency and safety in TKA in prior studies. The investigators performed a multicenter randomized controlled trial to determine the efficiency and safety of this technology in TKA. The investigators prospectively randomized 411 patients undergoing primary TKA to either barbed running (n=191) or knotted interrupted suture closure (n=203). Closure time was measured intraoperatively. Cost analysis was based on suture and operating room time costs.

Read the detailed description

Total knee arthroplasty (TKA) rates have consistently risen in recent years, and demand is expected to increase by over 600% in the next 20 years. Decreasing reimbursement and available resources make tangible advances in surgical efficiency and outcomes essential in meeting current and future demand. Closure time may be one of the best targets in the push to reduce operative time and cost while increasing operative productivity. Optimizing lengthy, multilayered wound closures in TKA is a promising means for improving both efficiency and outcomes by potentially decreasing wound closure time, reducing postoperative wound complications, and improving cosmetic outcomes.

Running knotless suture technique utilizing barbed suture technology has recently been shown to reduce wound closure time in both total hip and knee arthroplasty in a small, prospective, randomized clinical trial. Barbed suture technology has also facilitated rapid closure and soft-tissue repair in plastic-surgery literature. Very few studies have reported on the use of barbed suture technology for multilayered closure in orthopedics. As a pilot study, the investigators performed a retrospective analysis of consecutive cohorts before and after changing to barbed suture. The investigators believed that our published slight improvement in efficiency and cost savings of a barbed suture closure was underestimated due to the retrospective nature of our pilot study and the investigators therefore elected to proceed forward with a prospective randomized trial. Additionally, in the investigators pilot study we found a potential trend toward lower wound complications with the barbed suture and we wanted to see if this would be borne out in a prospective randomized trial.

The investigators hypothesized that a prospective study would show that barbed sutures would be more efficient, have comparable complication rates, clinical outcomes, and cosmesis outcomes versus traditional knotted sutures when used in the closure of primary TKA. Specifically, the investigators hypotheses were as follows: multilayered closure in TKA with barbed suture would be associated with (1) shorter closure times; (2) lower cost; (3) similar closure related perioperative complication rates; and (4) similar Knee Society, cosmesis, and patient satisfaction scores when compared to standard knotted suture closure.

02

Conditions studied

  • Arthropathy of Knee

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Keywords

  • barbed sutures
  • knotted sutures
  • total knee arthroplasty
  • knee surgery
03

In context

Joint Diseases

712 studies on the registry are indexed under Joint Diseases; 127 are open to participants now.

This study's enrollment of 363 is above the median of 100 across 216 observational studies indexed under Joint Diseases.

Browse Joint Diseases studies →

Lead sponsor

University of Utah is the lead sponsor of 969 studies on the registry; 178 are open to participants now.

Of its 107 completed or terminated interventional studies of FDA-regulated products, 62 (58%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study and control groups will be made up of consecutive patients undergoing a median parapatellar approach primary total knee arthroplasty at the University of Utah Hospital and Clinics. The control group will undergo two-layer closure utilizing a standard interrupted, knotted suture technique. The closures will be performed by 2 members of the team (attending surgeon, resident, fellow, or PA) in ALL closures so as to limit the possible confounder of closure time variation due to different numbers of people closing the incision. This will specifically consist of arthrotomy closure using interrupted #1 Ethibond™ in figure of eight fashion and sudermal closure using 2-0 Monocryl™ in interrupted buried fashion.

Inclusion criteria

  • Patients greater than 18 years of age
  • Undergoing primary total knee arthroplasty
  • English speaking

Exclusion criteria

Exclusion Criteria:

  • Patients less than 18 years of age
  • Prior open knee surgery in close proximity (\<2cm) to the proposed incision for the primary total knee arthroplasty (prior arthroscopic surgery does not exclude a patient from the study)
  • Wound or Scar in close proximity (\<2cm) to the proposed incision for the primary total knee arthroplasty
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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
363 participants (actual)

Groups and cohorts

  • Barbed sutures

    Barbed sutures are self-anchoring, requiring no knots for wound closure.

  • Knotted sutures

    Knotted sutures used for traditional surgical closures.

06

What researchers measure

Primary outcomes

  1. Intraoperative closure time in total knee arthroplasty.

    Time frame: 6 weeks

Secondary outcomes

  1. Cost analysis in terms of operative time and material costs of closure in total knee arthroplasty.

    Time frame: 6 weeks

07

Study locations

4 sites
  • Duke University Health System
    Durham, North Carolina 27710, United States
  • Joint Implant Surgeons Inc,
    New Albany, Ohio 43054, United States
  • Scott and White HealthCare
    Temple, Texas 76508, United States
  • University of Utah Orthopedics Center
    Salt Lake City, Utah 84106, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 4, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01320371
Lead sponsor
University of Utah
Responsible party
Christopher Peters (M.D., University of Utah) — Principal investigator
First posted
Mar 22, 2011
Start date
Jan 2011
Primary completion
Jan 2014
Completion
Jan 2014
Last update
Feb 4, 2014

Study contacts

Christopher Peters, MD
principal investigator · University of Utah hopsital
Jeremy Gililland, MD
principal investigator · University of Utah Orthopaedics Resident

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2014. You cannot join it, but the record below documents what was studied.

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