Skip to content

Bio ACL Reconstruction Amnion Collagen Matrix Wrap and Stem Cells

Pilot Study: Augmentation of ACL Reconstruction With Bone Marrow Stem Cells and Amnion Collagen Matrix Wrap

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03294759
Acronym
BioACLRCT
Enrollment
40
Registered
2017-09-27
Start date
2017-09-06
Completion date
2024-12-06
Last updated
2024-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ACL - Anterior Cruciate Ligament Rupture

Keywords

amion, stem cell, acl

Brief summary

Collagen based -membrane derived from amniotic tissue can be used to help reestablish the natural synovial lining of the reconstructed ACL, in effect acting as both a barrier from the synovial fluid and as a scaffold to contain autologous mesenchymal stem cells and growth factors contiguous with the graft, thus aiding and perhaps accelerating the natural maturation and ligamentization process of the implanted graft tissue. Acceleration and improvement in graft maturation and strength would be a significant advancement in sports medicine allowing safer and earlier return to sports and activity

Detailed description

Histologic studies have determined that graft ligamentization following anterior cruciate ligament (ACL) reconstruction may take from 6 to 18 months. (1) It has been reported that incomplete graft maturation and incorporation is one cause of clinical graft failure. Animal studies have illustrated improved tendon healing/integration in ACL models augmented with stem cell technologies. (2-4). Basic scientists theorize that optimization of stem cell treatments for tissue regeneration requires that a regenerative triad be employed, i.e., use of a scaffold, stem cells and growth factors. In the intra-articular environment, research has shown that a scaffold such as an amnion wrap is necessary to contain the stem cells and growth factors in close proximity to the ACL graft. (2, 4, 5) The normal, uninjured human ACL is covered by a layer of synovial tissue which contributes to the blood supply and nutrition of the native ACL. It is theorized that the lack of a synovial lining after injury and following traditional ACL reconstruction contributes to slow ligamentization and possible failure of reconstructed grafts.(5) Two studies have demonstrated accelerated maturation and ligamentization of human ACL graft augmented with point of care blood products. (6, 7) In one, leucocyte poor platelet rich plasma was injected directly into the body of the graft. (6) In the other, the platelet derived growth factors were loaded in a gelatin carrier which was wrapped around the graft. (7) In both studies accelerated and increased ligament maturation was documented compared to the controls. Collagen membranes derived from amniotic tissue have been successful to aid healing when used in difficult wounds and meniscal repair surgery. (8, 9) The use of a collagen based -membrane derived from amniotic tissue may be used to help reestablish the natural synovial lining of the reconstructed ACL, in effect acting as both a barrier from the synovial fluid and as a scaffold to contain autologous mesenchymal stem cells and growth factors contiguous with the graft. Thus aiding and perhaps accelerating the natural maturation and ligamentization process of the implanted graft tissue. Acceleration and improvement in graft maturation and strength would be a significant advancement in sports medicine allowing safer and earlier return to sports and activity.

Interventions

OTHERBio ACL

Bone marrow aspirate will be centrifuged using the Arthrex Angel system to optimally concentrate the cells for implantation. The graft for the experimental groups will be wrapped with a sterile amnion matrix wrap, supplied by Arthrex

OTHERControl

Normal ACL reconstruction technique with either patella or hamstring autograft

Sponsors

Arthrex, Inc.
CollaboratorINDUSTRY
Andrews Research & Education Foundation
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Bone marrow aspirate will be collected through the surgical site from the distal femur with a trocar designed for this purpose. Therefore patients will be unable to determine if they have had stem cells harvested

Intervention model description

ACL harvested for autograft reconstruction of the ACL with either hamstring or patellar tendon grafts. The graft will be wrapped in a collagen wrap and injection with aspirate from the patient's bone marrow. The control group will have standard ACL reconstruction with either hamstring or patellar tendon grafts.

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients between the ages of 18 and 45 who are scheduled to have anterior cruciate ligament reconstruction with autologous grafts by one of the investigating physicians will be screened for participation in this study. * Patients must be willing to undergo MRI scans post -operatively at 3, 6, 9 months and 1 year

Exclusion criteria

* Patients with prior procedures or significant prior injuries to the same knee are excluded. - - Any patient who will have difficulty obtaining internet access, does not have an active e-mail address, or is unable to comprehend study documents or give informed consent will be excluded. * Patient who are unable to complete MRI examinations due to claustrophobia or anxiety will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Changes in ACL3 months, 6 months, 9 months, 12 months post-opMRI region of interest mapping to produce mean T2 values

Secondary

MeasureTime frameDescription
Changes in patient-reported pain rating3 months, 6 months, 9 months, 12 months post-opVisual analog scale will be used to assess pain
Changes in Knee injury and Osteoarthritis Outcome Score (KOOS)3 months, 6 months, 9 months, 12 months post-opPatients will complete KOOS questionnaire on SOS
Changes in Short Form 12 (SF-12) patient ratings3 months, 6 months, 9 months, 12 months post-opPatients will complete SF-12 questionnaire on SOS
Changes in Single Assessment Numerical Evaluation (SANE) patient ratings for function3 months, 6 months, 9 months, 12 months post-opPatients will complete the SANE questionnaire on SOS
Marx Activity Scale Rating12 months post-opPatients will complete the Marx Activity questionnaire on SOS

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026