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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03148379
Other study ID # 20161119
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 11, 2017
Est. completion date March 30, 2022

Study information

Verified date June 2023
Source Medacta USA
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To compare economic factors and the rate of adverse events between two types of instrumentation used for total knee replacement: Single-use Efficiency Instruments with Patient Specific Technique (MyKnee®) Traditional Metal Instruments with Conventional Surgical Technique


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date March 30, 2022
Est. primary completion date March 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Age 18 to 75 years - BMI =35 - Undergoing unilateral total knee arthroplasty due to osteoarthritis (primary or post-traumatic OA) - Able and willing to give consent and to comply with study requirements, including follow up visit at 6 weeks Exclusion Criteria: - Pregnant women or those seeking to become pregnant. Pregnancy test is administered prior to surgery as part of routine care by the hospital / surgery center for all female patients of childbearing potential - Is participating in another clinical study - Has inflammatory arthritis - Has knee avascular necrosis - Has severe deformity, defined as greater than 10 degrees varus or valgus relative to the mechanical axis - Has retained hardware in the knee that requires removal or interferes with Total Knee Arthroplasty (TKA) procedure

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Customized patient instruments
Single use efficiency instruments and cutting blocks specifically made for each patient using pre-op MRI or CT scans to make bone cuts and select implant size.
Traditional Metal Instruments
Traditional metal instrument will be used to make bone cuts and size the components in this control group.

Locations

Country Name City State
United States Texas Orthopedics Austin Texas
United States Ortho Montana Billings Montana
United States Tandem Clinical Research, LLC Marrero Louisiana
United States Orthopedic Associates Meadville Meadville Pennsylvania
United States Jordan Valley Medical Center of Orthopedics Rehabilitation and Excellence West Jordan Utah

Sponsors (1)

Lead Sponsor Collaborator
Medacta USA

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary OR Total Time Total time patient is in operating room Day of Surgery
Primary Opening Instruments Time to open surgical instruments Day of Surgery
Primary Back Table Setup Time Time to set up back surgical table Day of Surgery
Primary Tourniquet Time Time tourniquet is on patient during surgery Day of Surgery
Primary Incision to Skin Closure Time from incision to skin closure during surgery Day of Surgery
Primary Bone Prep Time Time to prepare bone for implant during surgery Day of Surgery
Primary Patella Resection Time Time to resection patella during surgery Day of Surgery
Primary Clean-up Time Time to clean up following surgery Day of Surgery
Secondary Hemoglobin Range Post op 1 day hemoglobin range 24 hours or at discharge if patient does not stay overnight
Secondary Surgical Waste Weight Weigh surgical waste at the end of each surgery Day of Surgery
Secondary Mechanical Axis Radiographic analysis of mechanical axis alignment Pre-Operative
Secondary Mechanical Axis Radiographic analysis of mechanical axis alignment Post-Operative
Secondary Tibial Slope Radiographic analysis of Tibial Posterior Slope Pre-Operative
Secondary Tibial Slope Radiographic analysis of Tibial Posterior Slope Post-Operative
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