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Effect of ACP on Surgical Repair of Rotator Cuff Tears

Primary Purpose

Rotator Cuff Tears

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Autologous conditioned plasma
Control group
Sponsored by
Schulthess Klinik
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rotator Cuff Tears focused on measuring Rotator cuff tears, ACP

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Arthroscopic rotator cuff reconstructions of degenerative or traumatic full thickness rotator cuff tears (supraspinatus and/or infraspinatus tendon) performed by Dr. Flury and Dr. Schwyzer
  • Suture bridge technique
  • No pregnancy at the date of the surgery for women of childbearing potential
  • Signed consent form

Exclusion Criteria:

  • Partial reconstruction of the rotator cuff (PASTA)
  • Open reconstruction
  • Tendon transfer (latissimus dorsi or pectoralis major)
  • Revision surgery
  • Omarthrosis (Level ≥ 2 Samilson & Prieto)
  • Systemic arthritis
  • Rheumatoid arthritis
  • Diabetes (insulin treated)
  • Requiring surgery in reconstruction of the subscapularis tendon
  • Progressive fat inclusion (fatty infiltration of the rotator cuff musculature Goutallier level IV
  • Acute or chronic infection
  • Pathological bone metabolism
  • Insufficient perfusion in the affected arm
  • Neuromuscular disease in the affected arm
  • Non compliance of the patient
  • Disorders which handicap or inhibit the patient to follow the orders of the clinical testers

Sites / Locations

  • Schulthess Klinik

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

ACP treated

Control group

Arm Description

The patients are going to get an injection of 4mL autologous conditioned plasma under the footprint following an arthroscopic repair of the rotator cuff.

The patients are going to get an injection of 4mL saline solution under the footprint following an arthroscopic repair of the rotator cuff.

Outcomes

Primary Outcome Measures

Oxford Shoulder Score
The Oxford Shoulder Score used after 3 months is the primary parameter. The Score tests the ability to participate in the patients' normal life before they got injured.

Secondary Outcome Measures

VAS Pain
QuickDASH
EQ-5D
ROM
Measurement of the abduction strength
ASES Score
Constant Murley Score
MRI/X-Ray/Ultrasonic Diagnostics
Measurement of the external rotation strenght

Full Information

First Posted
December 22, 2010
Last Updated
May 19, 2015
Sponsor
Schulthess Klinik
Collaborators
Arthrex, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01266226
Brief Title
Effect of ACP on Surgical Repair of Rotator Cuff Tears
Official Title
Effect of Autologous Plasma (ACP) on Surgical Repair of Rotator Cuff Tears
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Completed
Study Start Date
December 2010 (undefined)
Primary Completion Date
February 2013 (Actual)
Study Completion Date
February 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Schulthess Klinik
Collaborators
Arthrex, Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if autologous plasma (ACP) is beneficial for better and faster healing following an arthroscopic repair of the rotator cuff.
Detailed Description
The shoulder joint, specially the rotator cuff, is one of the most complicated joints of the human body. If the tendon has to be fixed at the bone during surgery, the weak point in obtaining a successful surgery is the fixation of the tendon at the bone insertion site. Tendon belongs to the bradytrophic tissue conditional on the reduced blood flow, deep mitosis rate and lowered healing potential. We can boost the healing process with a selective use of PRP (platelet rich plasma). In this process, the healing site is delivered with an elevated concentration of thrombocytes and also growth factors which are constituent parts of them. In this study, we will test the Arthrex® Double Syringe System. With this system it is possible to obtain ACP (Autologous conditioned plasma) in one centrifugation step. The supernatant contains a concentration of thrombocytes which is twice as high as in the native blood. The concentration of the growth factors is 5-25x higher according to this. We also want to test if one application of ACP is enough to get a short- and long-term benefit in healing following a rotator cuff tear.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotator Cuff Tears
Keywords
Rotator cuff tears, ACP

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
129 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ACP treated
Arm Type
Experimental
Arm Description
The patients are going to get an injection of 4mL autologous conditioned plasma under the footprint following an arthroscopic repair of the rotator cuff.
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
The patients are going to get an injection of 4mL saline solution under the footprint following an arthroscopic repair of the rotator cuff.
Intervention Type
Device
Intervention Name(s)
Autologous conditioned plasma
Other Intervention Name(s)
ACP Arthrex
Intervention Description
4mL autologous conditioned plasma application under the footprint following an arthroscopic repair of the rotator cuff.
Intervention Type
Device
Intervention Name(s)
Control group
Other Intervention Name(s)
ACP Arthrex
Intervention Description
4mL saline application under the footprint following an arthroscopic repair of the rotator cuff.
Primary Outcome Measure Information:
Title
Oxford Shoulder Score
Description
The Oxford Shoulder Score used after 3 months is the primary parameter. The Score tests the ability to participate in the patients' normal life before they got injured.
Time Frame
3mo (6mo/24mo)
Secondary Outcome Measure Information:
Title
VAS Pain
Time Frame
10d po
Title
QuickDASH
Time Frame
3/6/24mo
Title
EQ-5D
Time Frame
3/6/24 mo
Title
ROM
Time Frame
3/6/24mo
Title
Measurement of the abduction strength
Time Frame
3/6/24 mo
Title
ASES Score
Time Frame
3/6/24mo
Title
Constant Murley Score
Time Frame
3/6/24 mo
Title
MRI/X-Ray/Ultrasonic Diagnostics
Time Frame
6/24 mo
Title
Measurement of the external rotation strenght
Time Frame
3/6/24 mo

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Arthroscopic rotator cuff reconstructions of degenerative or traumatic full thickness rotator cuff tears (supraspinatus and/or infraspinatus tendon) performed by Dr. Flury and Dr. Schwyzer Suture bridge technique No pregnancy at the date of the surgery for women of childbearing potential Signed consent form Exclusion Criteria: Partial reconstruction of the rotator cuff (PASTA) Open reconstruction Tendon transfer (latissimus dorsi or pectoralis major) Revision surgery Omarthrosis (Level ≥ 2 Samilson & Prieto) Systemic arthritis Rheumatoid arthritis Diabetes (insulin treated) Requiring surgery in reconstruction of the subscapularis tendon Progressive fat inclusion (fatty infiltration of the rotator cuff musculature Goutallier level IV Acute or chronic infection Pathological bone metabolism Insufficient perfusion in the affected arm Neuromuscular disease in the affected arm Non compliance of the patient Disorders which handicap or inhibit the patient to follow the orders of the clinical testers
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthias Flury, Dr
Organizational Affiliation
Upper Extremities Department
Official's Role
Principal Investigator
Facility Information:
Facility Name
Schulthess Klinik
City
Zürich
State/Province
Canton Zürich
ZIP/Postal Code
8008
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
27184542
Citation
Flury M, Rickenbacher D, Schwyzer HK, Jung C, Schneider MM, Stahnke K, Goldhahn J, Audige L. Does Pure Platelet-Rich Plasma Affect Postoperative Clinical Outcomes After Arthroscopic Rotator Cuff Repair? A Randomized Controlled Trial. Am J Sports Med. 2016 Aug;44(8):2136-46. doi: 10.1177/0363546516645518. Epub 2016 May 16.
Results Reference
derived

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Effect of ACP on Surgical Repair of Rotator Cuff Tears

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