CTRI/2019/10/021778
Not yet recruiting
Phase 4
Randomized Control Trial to compare the efficacy of, and patient satisfaction levels, following skin closure with surgical staples vs 2-Octyl Cyanoacrylate together with a Self Ahering Mesh (Dermabond Prineo) after unilateral Primary Total Knee Arthroplasty surgery in patients with osteoarthritis of the knee
Maxcure Medicover Hospital0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: M171- Unilateral primary osteoarthritisof knee
- Sponsor
- Maxcure Medicover Hospital
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients who are 18 years of age and above,
- •\-Patients undergoing Primary Total Knee Arthroplasty surgery for osteoarthritis of the knee
Exclusion Criteria
- •\-Age under 18 years
- •\-Known hypersensitivity to Dermabond Prineo Skin Closure System
- •\-Patients who have undergone any prior surgery to the knee planned for surgery
- •\-Patients with Inflammatory arthritis, crystalline arthropathy or secondary osteoarthritis of the knee
Outcomes
Primary Outcomes
Not specified
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