Clinical Analysis of a Novel Flexor Tendon Repair Technique, A Prospective Randomized Trial
Brett Lewellyn
Summary
The purpose of the research study is to determine the efficacy and efficiency of two tendon repair techniques: the CoNextions tendon repair device vs a standard of care, L-O (Lew-Omar), suture repair technique. The investigators will also determine if there are similar or different rates of complications and failures via both objective and subjective measures.
Description
To determine the tendon failure/rupture rate of two tendon repair techniques: the CoNextions tendon repair device vs a standard of care suture repair technique. The investigators will determine if there are similar or different rates of complications and failures (both intraoperatively and at 2-week, 6-week, 3-month, and 6-month post-operative intervals).
Eligibility
- Age range
- 22–88 years
- Sex
- All
- Healthy volunteers
- No
Inclusion Criteria: * Study subjects aged 22 and older. * Subjects who sustained a Zone 2-5 flexor tendon lacerations Exclusion Criteria: * Subjects under the age of 22 at the time of consent * Subjects who sustained a Zone 1 flexor tendon injury * Subjects who have had previous surgical procedures on the injured upper extremity. * Subjects who have metal allergies * Ischemia, blood supply compromise, and/or inadequate wound coverage * Prior or current infections at or near the implant site * Conditions which tend to limit the patient's ability or willingness to restrict activities or follo…
Location
- Orlando HealthOrlando, Florida