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Clinical Trials/CTRI/2019/10/021778
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Maxcure Medicover Hospital

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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