Mobile Technology to Assist Patient Education and Research in Arthroplasty

Medacta Australia0 个研究点目标入组 30 人开始时间: 2020年10月16日最近更新: 2020年10月26日

适应症

试验速览

暂无简介。

•Patients 18 years or over presenting with hip or knee arthritis that meets the indications for hip or knee arthroplasty respectively
•- Patients who are willing and able to provide written informed consent for participation in the study. Written informed consent must be obtained prior to the patient's surgery
•- Patients who are considered by the surgeon to be capable of following the patient optimised pathway

•- Patients under the age of 18 years
•- Patients with one or more medical conditions identified as a contraindication defined by the labelling on any Medacta implants used in this study
•- Any patient who cannot or will not provide informed consent for participation in the study
•- Patients who need revision surgery
•- Patients unable to communicate in English
•- Any case not described in the inclusion criteria
•- Patients who do not own a compatible smartphone

发起方

Medacta Australia