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Arthroscopic Superior Capsular Reconstruction - Study of Different Types of Grafts

Primary Purpose

Rotator Cuff Tear, Graft Complication

Status
Withdrawn
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Arthroscopic superior capsular reconstruction
Sponsored by
Hospital de Egas Moniz
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rotator Cuff Tear focused on measuring Arthroscopic Superior Capsular Reconstruction, Irreparable rotator cuff tear, Allograft, Autograft, Xenograft

Eligibility Criteria

40 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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)

Sites / Locations

  • Centro Hospitalar de Lisboa Ocidental

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

Fascia lata autograft

Fascia lata allograft

Achilles tendon allograft

Bovine pericardium allograft

Swine dermal xenograft

Collagen allograft

Arm Description

Arthroscopic superior capsular reconstruction using a fascia lata autograft

Arthroscopic superior capsular reconstruction using a fascia lata allograft

Arthroscopic superior capsular reconstruction using an achilles tendon allograft

Arthroscopic superior capsular reconstruction using a bovine pericardium allograft

Arthroscopic superior capsular reconstruction using a swine dermal xenograft

Arthroscopic superior capsular reconstruction using a collagen allograft

Outcomes

Primary Outcome Measures

Constant score
Constant score at 2 years postoperatively (minimum 1 point - maximum 100 points); For the scale range provided, higher values represent a better outcome

Secondary Outcome Measures

Graft integrity on the magnetic resonance imaging
Graft integrity on the 2-year postoperative magnetic resonance imaging (scale: 0 -1): 0 = graft absent or not healed to the greater tuberosity/superior glenoid; 1 = graft present and healed to the greater tuberosity and superior glenoid. For the scale range provided, higher values represent a better outcome.
Shoulder active range of motion
Shoulder active range of motion (ROM) at 2 years postoperatively measured in degrees using an analogic goniometer: elevation (0 - 180º), abduction (0 - 180º) and external rotation (0 - 100º); and internal rotation, defined as the highest vertebral body that the patient's thumb can reach, converted afterwards to a scale of 1 - 5 points: lateral thigh=0; buttock=1; sacrum=2; lumbar=3; 12th thoracic vertebra=4; 7th thoracic vertebra=5. For the scale range provided, higher values represent a better outcome.
Simple shoulder test
Simple shoulder test ((minimum 1 point - maximum 12 points) at 2 years postoperatively. For the scale range provided, higher values represent a better outcome.
Acromiohumeral interval
True anteroposterior shoulder radiograph at 2 years postoperatively: the acromiohumeral interval (AHI), considering the distance between the top of the humeral head and the undersurface of the acromion, measured using a software measurement tool (PACS, Agfa HealthCare); the RCT arthritis will be graded according to the Hamada revised radiographic classification. For the scale range provided, higher values represent a better outcome.
Shoulder strength
Shoulder strength at 2 years postoperatively measured in kilograms using a digital dynamometer: supraspinatus (0 - 25 kg).For the scale range provided, higher values represent a better outcome.

Full Information

First Posted
November 9, 2018
Last Updated
February 27, 2023
Sponsor
Hospital de Egas Moniz
Collaborators
Centro Hospitalar Lisboa Ocidental, General Hospital of Santo António, Centro Hospitalar De São João, E.P.E., Hospital Santa Maria Maior de Barcelos, CUF Santarém Hospital, Hospital de Braga, Centro Hospitalar e Universitário de Coimbra, E.P.E., Hospital Cuf Descobertas, Hospital Vila Franca de Xira
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1. Study Identification

Unique Protocol Identification Number
NCT03739749
Brief Title
Arthroscopic Superior Capsular Reconstruction - Study of Different Types of Grafts
Official Title
Arthroscopic Superior Capsular Reconstruction - Multicentric Prospective Comparative Study of Different Types of Grafts
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Withdrawn
Why Stopped
Multicenter failure
Study Start Date
October 30, 2018 (Actual)
Primary Completion Date
October 30, 2022 (Actual)
Study Completion Date
October 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital de Egas Moniz
Collaborators
Centro Hospitalar Lisboa Ocidental, General Hospital of Santo António, Centro Hospitalar De São João, E.P.E., Hospital Santa Maria Maior de Barcelos, CUF Santarém Hospital, Hospital de Braga, Centro Hospitalar e Universitário de Coimbra, E.P.E., Hospital Cuf Descobertas, Hospital Vila Franca de Xira

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotator Cuff Tear, Graft Complication
Keywords
Arthroscopic Superior Capsular Reconstruction, Irreparable rotator cuff tear, Allograft, Autograft, Xenograft

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Multiple group assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fascia lata autograft
Arm Type
Active Comparator
Arm Description
Arthroscopic superior capsular reconstruction using a fascia lata autograft
Arm Title
Fascia lata allograft
Arm Type
Active Comparator
Arm Description
Arthroscopic superior capsular reconstruction using a fascia lata allograft
Arm Title
Achilles tendon allograft
Arm Type
Active Comparator
Arm Description
Arthroscopic superior capsular reconstruction using an achilles tendon allograft
Arm Title
Bovine pericardium allograft
Arm Type
Active Comparator
Arm Description
Arthroscopic superior capsular reconstruction using a bovine pericardium allograft
Arm Title
Swine dermal xenograft
Arm Type
Active Comparator
Arm Description
Arthroscopic superior capsular reconstruction using a swine dermal xenograft
Arm Title
Collagen allograft
Arm Type
Active Comparator
Arm Description
Arthroscopic superior capsular reconstruction using a collagen allograft
Intervention Type
Procedure
Intervention Name(s)
Arthroscopic superior capsular reconstruction
Intervention Description
The superior capsule of patients with irreparable rotator cuff tears will be reconstructed using an autograft or an allograft
Primary Outcome Measure Information:
Title
Constant score
Description
Constant score at 2 years postoperatively (minimum 1 point - maximum 100 points); For the scale range provided, higher values represent a better outcome
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Graft integrity on the magnetic resonance imaging
Description
Graft integrity on the 2-year postoperative magnetic resonance imaging (scale: 0 -1): 0 = graft absent or not healed to the greater tuberosity/superior glenoid; 1 = graft present and healed to the greater tuberosity and superior glenoid. For the scale range provided, higher values represent a better outcome.
Time Frame
2 years
Title
Shoulder active range of motion
Description
Shoulder active range of motion (ROM) at 2 years postoperatively measured in degrees using an analogic goniometer: elevation (0 - 180º), abduction (0 - 180º) and external rotation (0 - 100º); and internal rotation, defined as the highest vertebral body that the patient's thumb can reach, converted afterwards to a scale of 1 - 5 points: lateral thigh=0; buttock=1; sacrum=2; lumbar=3; 12th thoracic vertebra=4; 7th thoracic vertebra=5. For the scale range provided, higher values represent a better outcome.
Time Frame
2 years
Title
Simple shoulder test
Description
Simple shoulder test ((minimum 1 point - maximum 12 points) at 2 years postoperatively. For the scale range provided, higher values represent a better outcome.
Time Frame
2 years
Title
Acromiohumeral interval
Description
True anteroposterior shoulder radiograph at 2 years postoperatively: the acromiohumeral interval (AHI), considering the distance between the top of the humeral head and the undersurface of the acromion, measured using a software measurement tool (PACS, Agfa HealthCare); the RCT arthritis will be graded according to the Hamada revised radiographic classification. For the scale range provided, higher values represent a better outcome.
Time Frame
2 years
Title
Shoulder strength
Description
Shoulder strength at 2 years postoperatively measured in kilograms using a digital dynamometer: supraspinatus (0 - 25 kg).For the scale range provided, higher values represent a better outcome.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
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)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Clara Azevedo
Organizational Affiliation
Centro Hospitalar de Lisboa Ocidental
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centro Hospitalar de Lisboa Ocidental
City
Lisboa
ZIP/Postal Code
1700-348
Country
Portugal

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
Citation
Lippitt S, Harryman DT, Matsen F. A pratical tool for function evaluation: the
Results Reference
background
PubMed Identifier
2323151
Citation
Patte D. Classification of rotator cuff lesions. Clin Orthop Relat Res. 1990 May;(254):81-6.
Results Reference
background
PubMed Identifier
3791738
Citation
Constant CR, Murley AH. A clinical method of functional assessment of the shoulder. Clin Orthop Relat Res. 1987 Jan;(214):160-4.
Results Reference
background
PubMed Identifier
18061114
Citation
Gilbart MK, Gerber C. Comparison of the subjective shoulder value and the Constant score. J Shoulder Elbow Surg. 2007 Nov-Dec;16(6):717-21. doi: 10.1016/j.jse.2007.02.123.
Results Reference
background

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Arthroscopic Superior Capsular Reconstruction - Study of Different Types of Grafts

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