Clinical Performance and Safety of the Unicompartmental Univation® XF Pro Implant

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorAesculap AG

About this trial

The study is designed as a prospective, observational, mid-term, multi-center follow-up study. It is planned to include 150 patients from 4 different study centres in Germany.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Indication for a primary medial unicompartmental knee endoprosthesis

Both cruciate ligaments intact

Lateral ligaments intact

Leg axis amenable to passive correction

Disqualifiers

Pregnancy

Patient age <18 and > 75 years

BMI ≥ 40

High risk patients ASA > III

Trial population

Patients between 18 and 75 years of age with an indication for a primary medial unicompartmental knee endoprosthesis

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • univation® XF Pro

    Device

    Primary medial unicompartmental knee arthroplasty

Treatment groups

150 Participants
are divided into 1 treatment group
Group A: univation® XF Pro1 intervention

Trial outcomes

Primary outcomes

1

Functional patient-reported outcome

The Oxford Knee Score (OKS) is a reliable 12-item, patient-reported questionnaire originally developed and validated specifically to assess function and pain in patients undergoing total knee replacement. It is short, reproducible, valid and sensitive to clinically important changes over time. Each of the 12 questions on the OKS is scored in the same way with the score decreasing as the reported symptoms increase (i.e. become worse). All questions are laid out with response categories denoting least (or no) symptoms to the left of the page (scoring 4) and those representing greatest severity lying on the right hand side (scoring 0), as detailed for question 1 below. This method, when summed, produces overall scores running from 0 to 48 with 48 being the best outcome.

Time frame
5 years post-op

Secondary outcomes

1

Implant survival [Kaplan-Meier]

Kaplan-Meier Analysis is a standard statistical method to describe the survival of human subjects or medical products over a defined time period.

Time frame
until 5 years postoperatively
2

Quality of Life [EQ-5D-5L] compared to baseline

The 5-dimension 5-level measure of the health status, developed by the EuroQol Group (EQ-5D-5L) is a simple and generic measure for clinical and economic assessment. Instructions for the user are directly included into the questionnaire and it consists of two pages. One cover five different dimensions (mobility, self care, usual activities, pain/discomfort, anxiety/depression) and the other one the EQ visual Analogue Scale (EQ-VAS). The VAS scale records the self rated health status of the patient from the level "the worst health you can imagine" to "the best health you can imagine". The answer of each of the five dimensions result in a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state.

Time frame
Preoperatively (baseline) and 3 months, 1 year, 2 years, 5 years postoperatively
3

Progress of Clinical Outcome [Forgotten Joint Score-12] over follow-up period

The Forgotten Joint Score-12 (FJS-12) Knee was designed to assess patient outcome in patients undergoing conservative or operative treatment of the knee. These Patient Reported Outcome (PRO) questionnaires focus on patients' awareness of a specific joint in everyday life. In 12 Items the awareness for the artificial joint is assessed by the patient, each on a five point scale (Never / Almost Never / Seldom / Sometimes / Mostly) The Forgotten Joint Score assessment consists of 12 questions and is scored on a 0-100 scale. The higher the score, the less the patient is aware of their affected joint when performing daily activities

Time frame
3 months, 1 year, 2 years, 5 years postoperatively
4

Radiological assessment: axis alignment (long leg x-ray) over time

Radiographs shall be standardized between centres as far as possible. Unless limited by patient or equipment constraints, all follow-up imaging examinations will be obtained according to the radiographic protocol of the hospital and the set routine. The radiographic evaluation of Alignment is based on long-leg x-rays

Time frame
at discharge (approx. 7-10 days postoperatively), 3 months, 1 year, 2 years, 5 years postoperatively

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Aesculap AG

Lead sponsor

Raylytic GmbH

Collaborator