Arthroscopic Superior Capsular Reconstruction - Multicentric Prospective Comparative Study of Different Types of Grafts
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Rotator Cuff Tear
- Sponsor
- Hospital de Egas Moniz
- Locations
- 1
- Primary Endpoint
- Constant score
- Status
- Withdrawn
- Last Updated
- 3 years ago
Overview
Brief Summary
Multicentric prospective clinical and radiological comparative study of consecutive patients with irreparable rotator cuff tears to test the hypothesis that there are significant differences in the improvement of the clinical and imaging outcomes of arthroscopic superior capsular reconstruction (ASCR) when a different type of graft is used.
Detailed Description
Patients with irreparable rotator cuff tears who meet the eligibility criteria will be enrolled in the study and undergo arthroscopic superior capsular reconstruction using one of the following types of graft: fascia lata autograft, fascia lata allograft, Achilles tendon allograft, bovine pericardium xenograft, swine dermal xenograft, or collagen graft. All patients will be assessed clinically, radiologically and with an MRI preoperatively and at the 6-months and at the 2-years postoperative evaluations. The range of motion (ROM), shoulder abduction strength, Constant (CS), simple shoulder test (SST) and subjective shoulder value (SSV) scores will be compared from preoperative to 6 months postoperative; from 6 months postoperative to 2 years postoperative (paired-samples t-test, two-tailed) in each group (allotment to groups is performed according to the type of graft used: fascia lata autograft, fascia lata allograft, Achilles tendon allograft, bovine pericardium xenograft, swine dermal xenograft, or collagen graft). The differences in ROM, shoulder abduction strength, CS, SST and SSV scores from preoperative to 6 months postoperative and from 6 months postoperative to 2 years postoperative will be compared between groups. All continuous variables will be compared between the group of patients with graft tears and the group without graft tears (Mann-Whitney U test). All categorical variables and outcome results will be compared between groups (Fisher's exact test). A significant difference will be defined as P\<0.05.
Investigators
Clara Isabel de Campos Azevedo
Principal Investigator
Hospital de Egas Moniz
Eligibility Criteria
Inclusion Criteria
- •Rotator cuff tear arthropathy, Hamada stage 1 or 2
- •Complete rotator cuff tendon tear involving one or more tendons, with a Patte stage 3 tendon retraction on the preoperative magnetic resonance imaging
Exclusion Criteria
- •Rotator cuff tear arthropathy, Hamada stage 3 or 4
- •Complete rotator cuff tendon tear involving one or more tendons, with Patte stage 1 or 2 tendon retraction on the preoperative magnetic resonance imaging
- •Proximal humerus fracture
- •Acute shoulder dislocation (in the previous 8 weeks)
Outcomes
Primary Outcomes
Constant score
Time Frame: 2 years
Constant score at 2 years postoperatively (minimum 1 point - maximum 100 points); For the scale range provided, higher values represent a better outcome
Secondary Outcomes
- Simple shoulder test(2 years)
- Shoulder strength(2 years)
- Graft integrity on the magnetic resonance imaging(2 years)
- Shoulder active range of motion(2 years)
- Acromiohumeral interval(2 years)