Clinical Trials Directory

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UnknownNCT04506580

Comparison of Postoperative Wound Between Dermabond Prineo(2-octyl Cyanoacrylate Adhesive and Polyester Mesh) and Subcuticular Suture in Simultaneous Total Knee Arthroplasty

Comparison of Postoperative Wound Between Dermabond PRINEO™(2-octyl Cyanoacrylate Adhesive and Polyester Mesh) and Subcuticular Suture in Simultaneous Total Knee Arthroplasty

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
The Catholic University of Korea · Academic / Other
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

This study aims to compare the clinical results of postoperative wound between Dermabond PRINEO™(2-octyl Cyanoacrylate adhesive and polyester mesh) and subcuticular suture in simultaneous total knee arthroplasty There is previous studies over whether or not to use skin adhesive material is superior or inferior to subcuticular suture This study prospectively randomized patients receiving bilateral total knee arthroplasty(TKA). Patients preference and clinical results was investigated in both knee of same patients who received skin adhesive or subcuticular suture in each knee.

Conditions

Interventions

TypeNameDescription
PROCEDUREDERMABOND™ PRINEO™(2-octyl Cyanoacrylate Adhesive and Polyester Mesh) vs subcuticular nylon sutureDERMABOND™ PRINEO™(2-octyl Cyanoacrylate Adhesive and Polyester Mesh) and subcuticular nylon suture are applied for each knee

Timeline

Start date
2019-03-06
Primary completion
2020-07-01
Completion
2020-07-30
First posted
2020-08-10
Last updated
2020-08-10

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT04506580. Inclusion in this directory is not an endorsement.