Status:
UNKNOWN
Comparison of Postoperative Wound Between Dermabond Prineo(2-octyl Cyanoacrylate Adhesive and Polyester Mesh) and Subcuticular Suture in Simultaneous Total Knee Arthroplasty
Lead Sponsor:
The Catholic University of Korea
Conditions:
Osteoarthritis, Knee Cutaneous Suture, Dermabond, Subcuticular Suture
Eligibility:
All Genders
19+ years
Phase:
NA
Brief 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 a...
Eligibility Criteria
Inclusion
- Patients for total knee arthroplasty
- having medicare insurance
Exclusion
- Rheumatoid arthritis
- Other inflammatory arthritis
- Neuropsychiatric patients
- Allergy or intolerance to study material
- Patients with an American Society of Anesthesiologists(ASA) score of IV (angina, congestive heart failure, dementia, cerebrovascular accident)
Key Trial Info
Start Date :
March 6 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 30 2020
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT04506580
Start Date
March 6 2019
End Date
July 30 2020
Last Update
August 10 2020
Active Locations (1)
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1
Seoul St. Mary's Hospital
Seoul, South Korea, 06591