Ignite Creation Date:
2024-05-06 @ 7:53 PM
Last Modification Date:
2024-10-26 @ 3:16 PM
Study NCT ID:
NCT06178380
Status:
RECRUITING
Last Update Posted:
2024-01-23
First Post:
2023-11-03
Brief Title:
Instrumental Versus Standard Rehabilitation for Knee Osteoarthritis
Sponsor:
Mohammed V Souissi University
Organization:
Mohammed V Souissi University
Study Overview
Official Title:
Clinical and Instrumental Biomechanical Assessement and Rehabilitation of Patients With Knee OsteoarthritisA Randomized Single Blind Clinical Trial
Status:
RECRUITING
Status Verified Date:
2023-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
A randomized clinical trial to evaluate the effectiveness of an instrumental rehabilitation protocol compared with standard protocol In patients with knee osteoarthritis
Detailed Description:
This is a randomized clinical trial designed to compare two intervention aimed at reducing and improving knee function in patients with knee osteoarthritis
- sixty subjects suffering from knee osteoarthritis will be recruited 30 per group
A instrumental rehabilitation Bstandard rehabilitation All patients who meet the clinical inclusion and exclusion criteria will have a standard radiography
selected patients will be invited to participate and will be informed of the purpose and conduct of the study
patients will be randomized to either the instrumental rehabilitation programme groupe or the standard rehabilitation group
patients in both groups will have a protocol that will be extended over 6 weeks
participants will be assessed primarily for function and pain as well as other secondary endpoints at baseline at 3 weeks and at 12 weeks
- sixty subjects suffering from knee osteoarthritis will be recruited 30 per group
A instrumental rehabilitation Bstandard rehabilitation All patients who meet the clinical inclusion and exclusion criteria will have a standard radiography
selected patients will be invited to participate and will be informed of the purpose and conduct of the study
patients will be randomized to either the instrumental rehabilitation programme groupe or the standard rehabilitation group
patients in both groups will have a protocol that will be extended over 6 weeks
participants will be assessed primarily for function and pain as well as other secondary endpoints at baseline at 3 weeks and at 12 weeks
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None