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Preloading of the braid with 300 N was performed prior to its fixation to the DIS device at a pretension of 80 N in 10° flexion.
With this technique, a polyethylene braid with a preassembled button is anchored to the femur and clamped to the DIS device, which is screwed into the tibial head.
The DIS device (Ligamys, Mathys Ltd. Bettlach, Switzerland) was implanted according to the operations manual using a small medial arthrotomy after dissection of the ACL with a scalpel at its femoral footprint.
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A patent application for "Con-Dis" device is currently pending.
TR was responsible for designing and building the Con-Dis device and providing help with the Con-Dis device.
A detailed description of the Con-Dis device has been provided elsewhere [ 10].
Some misinterpretations of the instructions on how to use the Con-Dis device were noticed.
The data were collected from the Con-Dis device by using a (SD) memory card.
The Con-Dis device functioned well in the present field study.
The Con-Dis device was invented recently and the methodology has already been published elsewhere earlier [ 10].
Before the test period, the test subjects were trained by a nurse to use the Con-Dis device and to fill out the RAI questionnaire.
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