Ignite Creation Date:
2024-05-06 @ 8:16 PM
Last Modification Date:
2024-10-26 @ 3:24 PM
Study NCT ID:
NCT06316050
Status:
COMPLETED
Last Update Posted:
2024-03-18
First Post:
2024-01-16
Brief Title:
Retrovertion Assesment and Study in Elderly Patients With Reverse Total Shoulder Arthroplasty
Sponsor:
Consorci Sanitari de Terrassa
Organization:
Consorci Sanitari de Terrassa
Study Overview
Official Title:
Retrovertion Assesment and Study of the Subscapularis Function in Elderly Patients With Reverse Total Shoulder Arthroplasty
Status:
COMPLETED
Status Verified Date:
2024-02
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:
Determine the optimal degree of retroversion 0-30º to obtain the best rotational mobility both internal and external of the shoulder after implanting a reversed sghoulder arthroplasty Comprehensive system and analyze the functional and radiologic results based on humeral retroversion
Detailed Description:
Methodology Open randomized controlled clinical trial It will be carried out with patients operated with reverse shoulder arthroplasty at 0º and 30º of humeral retroversion included consecutively in Terrassa Hospital from January 2019 to June 2021 The estimated sample will be 30 patients per group with diagnosis of massive rotator cuff rupture rotator cuff arthropaty and primary osteoarthritis with cuff injury with Walchs type B2 glena or in patients older than 80 years A global study will be carried out preoperatively and postoperatively with radiographs computerized tomography magnetic resonance and a biomechanical study
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