Ignite Creation Date:
2024-05-06 @ 4:04 PM
Last Modification Date:
2024-10-26 @ 2:03 PM
Study NCT ID:
NCT04867746
Status:
COMPLETED
Last Update Posted:
2021-12-08
First Post:
2021-04-27
Brief Title:
Clinical and Functional Outcomes at Least 2 Years After Hamstring Muscle Repair
Sponsor:
University Hospital Basel Switzerland
Organization:
University Hospital Basel Switzerland
Study Overview
Official Title:
HamRepair Clinical and Functional Outcomes at Least 2 Years After Hamstring Muscle Repair
Status:
COMPLETED
Status Verified Date:
2021-12
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:
HamRepair
Brief Summary:
This study is to evaluate functional outcomes of a new intraoperative lateral positioning of the anchors on the tuber ischiadicum in comparison to regular anatomical anchoring direct on top of the tuber ischiadicumafter hamstring muscle repair This study is to quantify at least 2 years postoperative functional biomechanical and clinical outcomes including side-to-side differences in muscle strength unipedal balance gait jumping and squatting function muscle activity in patients treated by hamstring muscle repair
Detailed Description:
The design of this pilot study is a descriptive cross-sectional single centre analysis involving all patients previously treated with hamstring repair All of these patients will be asked to participate in clinical and detailed functional analysis at least 2 years after surgery Specifically biomechanical and functional data including isokinetic muscle strength clinical scores ROM joint kinematics and kinetics during walking running squatting and single leg jumps muscle activity and single leg balance ability in the affected and contralateral leg will be collected These parameters will be compared between legs and correlated with clinical scores
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