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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03605290
Other study ID # 003418EMC
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 15, 2018
Est. completion date January 1, 2020

Study information

Verified date February 2020
Source HaEmek Medical Center, Israel
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Advance Knee osteoarthritis is treated by Total knee replacement. Since the first TKR in 1973 there has been continuous advance in implant technology as well as operative technique, yet current patient satisfaction after the procedure is accepted to be about 80%.

There are a few operative techniques to perform TKR. Until recently the most common technique is the anterior approach to the knee and then using mechanical instrumentation to make the bone cuts for the femur and tibia. A second popular technique is the anterior approach to the knee and then using a kinematic alignment to make the bone cuts.

The investigators wish to compare short term results of the two operative techniques as evidenced in patient objective functional scores and also by evaluating the gait of the patients by using the REHAGAIT ANALYZER PRO by HASOMED inc. Magdeburg Germany.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date January 1, 2020
Est. primary completion date January 1, 2020
Accepts healthy volunteers No
Gender All
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients after total knee replacement which was performed in our ward.

Exclusion Criteria:

- Less than 6 months have passed after the procedure

- Inability to understand and fill out PROMS questionnaires.

- Inability to walk without aids for at least 20 meters.

Study Design


Intervention

Diagnostic Test:
REHAGAIT ANYLIZER
Gait analysis instrumentation

Locations

Country Name City State
Israel haemek MC Afula

Sponsors (1)

Lead Sponsor Collaborator
HaEmek Medical Center, Israel

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary PROMS The patients will fill out functionala and quality of life assessment questionnaires At least 6 months post operatively
Primary Gait analysis The patients will perform a gait analysis using the REHAGAIT system. At least 6 months post operatively
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