Assessment of the Safety and Performance of a Compression Knee Support in the Prevention of Injuries During Sports Practice

Terminated

• Conditions: Chronic Knee Pain; Chronic Instability of Knee Joint

• Registration Number: NCT04601168
• Lead Sponsor: Decathlon SE

Brief Summary

Decathlon has developed kneeSOFT100 product which is medical device designed to reduce pain and joint instability during sport practice. The objective of this multicentre study is to collect data on the related clinical complications and clinical outcomes of market-approved Decathlon kneeSOFT100 product to demonstrate safety and performance of this device in a real-world setting.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2020-09-04
• Study First Submitted QC: 2020-10-22
• Study First Posted: 2020-10-23
• Study Start: 2021-03-25
• Primary Completion: 2022-07-19
• Study Completion: 2022-07-19
• Status Verified: 2022-09
• Last Update Submitted: 2022-09-12
• Last Update Posted: 2022-09-14

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 7

Inclusion Criteria

• Subject is aged ≥18 years old
• Subject has chronic pain AND / OR chronic knee instability
• The current condition of his/her knee allows the subject to resume usual physical activity
• Subject has been informed and is willing to sign an informed consent form
• Subject is willing to comply with protocol requirements and return to the study center for all clinical evaluations and required follow-up (6 weeks)
• Subject is affiliated to the French social security regime

Exclusion Criteria

• Subject has conditions that may interfere with his/her ability to understand protocol requirements, participate in scheduled visits, or provide his/her informed consent
• Subject has worn a support (knee brace or articulated orthosis) during sports sessions during the last month
• Subject has any medical condition that could impact the study at investigator's discretion
• Subject has a known hypersensitivity or allergy to the components of the device (elastodiene, polyester)
• Adult subject to a legal protection measure

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Functional score	6 weeks of follow-up	Comparison of the functional result (Lysholm Score: 0-100 points) between the baseline and last follow-up visit

Secondary Outcome Measures

Name	Time	Method
Confidence level	At baseline and 6 weeks of follow-up	Gap in the confidence level (patient rated outcome with 6 questions, ranging from 0 to 100) related to physical activity, between the baseline and last follow-up visit
Knee instability	At 2 weeks and 6 weeks of follow-up	Comparison of knee instability between the first two weeks of follow-up (without use of the device during sports sessions) and the following four weeks (with use of the device during sports sessions), measured through a numerical rating scale (NRS, ranging from 0 to 10)
Knee pain	At 2 weeks and 6 weeks of follow-up	Comparison of knee pain between the first two weeks of follow-up (without use of the device during sports sessions) and the following four weeks (with use of the device during sports sessions), measured through a NRS (ranging from 0 to 10)
Safety (adverse events)	6 weeks of follow-up	Rate of adverse events occurred during the study

Trial Locations

Locations (2)

KOSS Paris 8; 🇫🇷 Paris, France

Centre Hospitalier Universitaire de Lille; 🇫🇷 Lille, France