[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT04650568":3,"trial-entities:NCT04650568":107,"trial-summary:NCT04650568":111},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":7,"overall_status":8,"completion_date":9,"status_verified_date":10,"last_update_date":11,"start_date":12,"sponsor_name":13,"lead_sponsor_class":14,"has_dmc":15,"brief_summary":16,"detailed_description":17,"conditions":18,"keywords":21,"study_type":28,"primary_purpose":29,"phases":30,"enrollment_info":32,"interventions":35,"primary_outcomes":49,"secondary_outcomes":54,"sex":67,"minimum_age":68,"maximum_age":69,"healthy_volunteers":15,"eligibility_criteria":70,"std_ages":92,"locations":94,"central_contacts":103,"overall_officials":104,"references":105,"see_also_links":106},"NCT04650568","17082504","Biologic Augmentation With Mesenchymal Stem Cells in Patients Undergoing Anterior Cruciate Ligament Reconstruction","A Prospective Randomized Trial of Biologic Augmentation With Mesenchymal Stem Cells in Patients Undergoing Anterior Cruciate Ligament Reconstruction","ENROLLING_BY_INVITATION","2027-12-31","2026-06","2026-06-18","2017-11-03","Rush University Medical Center","OTHER",false,"This study will evaluate the efficacy of biologic augmentation of ACL reconstruction with bone marrow derived mesenchymal stem cells as measured by magnetic resonance imaging to detect graft healing and integration. Secondary endpoints will include validated patient reported outcome measures, as well as functional outcome using objective examination findings.","Introduction\n\nAnterior cruciate ligament (ACL) tears are a common and devastating injury among young athletes, and re-injury poses significant threats to both successful return to play and long term outcomes. Graft healing during ACL reconstruction (ACLR) is a slow biologic process, that involves graft incorporation into bone tunnel sites, as well as intra-articular graft remodeling . The intra-articular graft remodeling process is known as ligamentization, and occurs in three phases after ACLR. The first phase of early healing occurs between 0 and three months, the second phase occurs between 6 months and one year, and the final phase of maturation occurs after 1 year when the graft appears very similar to the native ACL. The studies that defined these time points biopsied human bone-patella tendon-bone (BTB) ACL autografts at different postoperative points, and described changes occurring over time in regards to vascularization, cellular aspects, and appearance of the extracellular matrix in comparison to control ACLs . Unlike animal models which display a necrotic stage, grafts in human models undergo an early vascular invasion, associated with fibroblasts that are converted to a hyper-cellular matrix with only focalized areas of necrosis . This process occurs as early as 3 weeks postoperatively, and increases over time as areas similar to the native patellar tendon with mature collagen and metabolically quiescent cells decrease . This process is the limiting factor in graft healing for bone-patella tendon-bone (BTB) grafts, as osteointegration occurs earlier .\n\nThe processes of osteointegration and ligamentization are responses to the new intrasynovial milieu and physical forces that the new graft is exposed to. During these healing and restructuring processes, failure load and stiffness of grafts decreases by up to 24% at 7 weeks, before strengthening to their potential . This contributes to the long recovery period for ACLR, and the risk of re-rupture during this period. Advances in biologic adjuncts to accelerate and improve this healing process would have a significant impact on the management of ACL injuries.\n\nRecently, biologic preparations of various growth factors have been developed to safely and effectively treat a variety of musculoskeletal conditions, including tendinopathies and arthritis . Bone marrow aspirate concentrate (BMAC) consists of undifferentiated mesenchymal stem cells that are concentrated and applied to the injury site . Previous studies have demonstrated this treatment to offer the pluripotent potential of the cells to impact healing, regeneration, biomechanical strength, and reducing bone-tunnel enlargement . Investigators have demonstrated that mesenchymal stem cell reinforced grafts had a significantly higher failure load and stiffness as early as 8 week post-operation in a rabbit model, suggesting an added benefit of advanced healing . Using BMSCs can offer a novel method to enhance tendon graft osteointegration. While there have been numerous laboratory studies researching the effect of mesenchymal stem cells, there lacks evidence in translation to the clinical setting. Silva et al performed a study where they injected bone marrow derived stem cells (BMSCs) into patellar tendon grafts to examine for increased graft-to-bone tunnel integration. They did not find a significant difference of tunnel integration on MRI imaging, but they did not examine the intra-articular portions for the effect on the ligamentization process, nor did they examine the effect on clinical examination and patient reported outcomes .\n\nQuantitative MRI is a non-invasive method to interrogate tissue properties and evaluate the biochemical composition of tissues. The T2\\* sequence gives information regarding tissue graft volume, water content, fiber alignment, and tissue density. Median grayscale values (a measure to determine tissue quality)can also be correlated to maximum failure load, yield load, and linear stiffness of grafts in a porcine model. Increases in MRI signals in ACL grafts have been found to be time dependent, becoming well established by three months, particularly at the distal intra-articular portion near the tibial tunnel . These changes have not been shown previously to be predictive of graft failure, but Investigators have recently also confirmed that normalized T2\\* signal intensity values of ACL grafts have significant correlation with knee instability related to ligamentization and tunnel healing.\n\nA recent study examined intra-articular graft maturation after platelet-rich plasma gel (PRPG) application, with MRI at month intervals from 3-12 months postoperatively. The intra-articular segment was divided in a proximal, middle, and distal segment, on a scale from 0-3 ranging from completely homogenous to severely heterogeneous. The mean time to obtain completely homogenous bone-patella tendon-bone (BTB) graft was 109 days for the PRPG group, and 363 for the control group 8.\n\nWe propose using quantitative magnetic resonance (MR) imaging with T2\\* mapping to investigate if BMAC treatment at time of ACL reconstruction can accelerate the graft maturation and healing process. We will perform a randomized controlled trial of patients undergoing ACL reconstruction with bone-patellar tendon-bone allograft evaluating the T2\\* weighted MRI changes of the graft at 3 and 9 months after surgical reconstruction. Additionally, we will obtain patient-reported outcome measures from this cohort to evaluate if BMAC treatment imparts a clinically-significant effect on ACL reconstruction.\n\nStudy Rationale\n\nThis study will evaluate the efficacy of biologic augmentation of ACL reconstruction with BMSCs as measured by magnetic resonance imaging to detect graft healing and integration. Secondary endpoints will include validated patient reported outcome measures, as well as functional outcome using objective examination findings.\n\nHypothesis\n\nThe hypotheses of this study are that there will be improved graft healing and integration at three and nine months as measured by decreased signal intensity and heterogeneity on T2\\* MRI following administration of BMAC during ACL reconstruction compared to the control group. Additionally, patient reported outcomes and physical examination findings will be significantly improved at an earlier time in those who receive the BMAC treatment to their allograft compared to the control group.\n\nStudy Plan\n\nThis study will be a prospective randomized trial of patients undergoing arthroscopic reconstruction of full thickness anterior cruciate ligament (ACL) tears. All patients who sign consent and undergo full thickness ACL reconstruction will be enrolled in the study. Enrollment will continue until 32 patients, 16 in each group, are enrolled. Follow-up will take place at 6 weeks, 3 months, 6 months, 9 months, 12 months, and 24 months.",[19,20],"Anterior Cruciate Ligament Injury","Anterior Cruciate Ligament Rupture",[22,23,24,25,26,27],"Anterior Cruciate Ligament","ACL","Stem Cell","Mesenchymal stem cells","biologic","augmentation","INTERVENTIONAL","TREATMENT",[31],"NA",{"count":33,"type":34},100,"ESTIMATED",[36,44],{"type":37,"name":38,"description":39,"armGroupLabels":40,"otherNames":42},"DEVICE","Autologous Bone Marrow Derived Mesenchymal Stem Cells","Autologous Bone Marrow Derived Mesenchymal Stem Cells injected into the ACL allograft prior to graft implantation.",[41],"Mesenchymal Stem Cell Recipient",[43],"Sham Incision",{"type":14,"name":45,"description":46,"armGroupLabels":47},"Sham incision","Small incision over the site where bone marrow aspirate would have been obtained",[48],"Control Sham Incision",[50],{"measure":51,"description":52,"timeFrame":53},"Signal to Noise Quotient","Signal intensity of the ACL graft on T2 weighted MRI imaging compared to a reference structures' signal intensity","9 months",[55,59,63,65],{"measure":56,"description":57,"timeFrame":58},"Side to side difference in anterior tibial translation","Anterior tibial translation measured by (Knee laxity Testing device) KT-1000 Arthrometer","6 weeks, 3 months, 6 months, 9 months, 1 year",{"measure":60,"description":61,"timeFrame":62},"Patient reported outcomes- Tegner Score","Patient reported outcome measure for patients receiving arthroscopic knee surgery","3 months, 6 months, 9 months, 12 months, 24 months",{"measure":64,"description":61,"timeFrame":62},"Patient reported outcomes- Knee Injury and Osteoarthritis Outcome Score for Joint Replacement (KOOS Jr)",{"measure":66,"description":61,"timeFrame":62},"Patient reported outcomes- International Knee Documentation Committee (IKDC) Score","ALL","18 Years","60 Years",{"inclusion":71,"exclusion":75,"raw_text":91},[72,73,74],"English-speaking patients","18-60 years of age with acute ACL injury (\\\u003C6 months from time of injury to reconstruction) and undergoing reconstruction with patellar tendon allograft","Written informed consent is obtained",[76,77,78,79,80,81,82,83,84,85,86,87,88,89,90],"Revision Surgery","Prior history of knee surgery","Concomitant ligamentous injury","Inability to obtain an MRI","Inability to participate in follow-up for the study","Any patient lacking decisional capability","Diagnosed musculoskeletal cancer or any diagnosed cancer, other than","musculoskeletal if not on long term remission (e.g. at least 5 years or negative biopsy at last exam), except basal cell carcinoma","Patients who are at higher risk for post-surgical bleeding (e.g., bleeding disorder taking anticoagulants except low dose aspirin) or post-surgical infection (e.g., taking immunosuppressants; have a severe infection or a history of serious infection or use of systemic steroids)","Known history of HIV, or has active Hepatitis B or active Hepatitis C","Alcohol and drug (medication) abuse","Pregnant or breast feeding women. Pregnancy as determined by a positive pregnancy test prior to procedure. Females of childbearing potential must agree to use an acceptable birth control method during study participation.","Patients that have received PRP, other platelet-based product, or investigational treatment in another cell\u002Fbiologic study for the target knee in the 12 months prior to the injection procedure","Any clinically significant finding that would place the patient at health risk, impact the study, or affect the completion of the study","Any psychiatric illness that would prevent comprehension of the details and nature of the study and interfere with follow-up clinic visits","Inclusion Criteria:\n\n* English-speaking patients\n* 18-60 years of age with acute ACL injury (\\\u003C6 months from time of injury to reconstruction) and undergoing reconstruction with patellar tendon allograft\n* Written informed consent is obtained\n\nExclusion Criteria:\n\n* Revision Surgery\n* Prior history of knee surgery\n* Concomitant ligamentous injury\n* Inability to obtain an MRI\n* Inability to participate in follow-up for the study\n* Any patient lacking decisional capability\n* Diagnosed musculoskeletal cancer or any diagnosed cancer, other than\n* musculoskeletal if not on long term remission (e.g. at least 5 years or negative biopsy at last exam), except basal cell carcinoma\n* Patients who are at higher risk for post-surgical bleeding (e.g., bleeding disorder taking anticoagulants except low dose aspirin) or post-surgical infection (e.g., taking immunosuppressants; have a severe infection or a history of serious infection or use of systemic steroids)\n* Known history of HIV, or has active Hepatitis B or active Hepatitis C\n* Alcohol and drug (medication) abuse\n* Pregnant or breast feeding women. Pregnancy as determined by a positive pregnancy test prior to procedure. Females of childbearing potential must agree to use an acceptable birth control method during study participation.\n* Patients that have received PRP, other platelet-based product, or investigational treatment in another cell\u002Fbiologic study for the target knee in the 12 months prior to the injection procedure\n* Any clinically significant finding that would place the patient at health risk, impact the study, or affect the completion of the study\n* Any psychiatric illness that would prevent comprehension of the details and nature of the study and interfere with follow-up clinic visits",[93],"ADULT",[95],{"facility":13,"city":96,"state":97,"zip":98,"country":99,"geoPoint":100},"Chicago","Illinois","60521","United States",{"lat":101,"lon":102},41.85003,-87.65005,[],[],[],[],{"nct_id":4,"conditions":108,"biomarkers":110},[109],"Injury of anterior cruciate ligament",[],{"nct_id":4,"found":112,"summary":113,"prompt_version":123},true,{"design":114,"status":115,"heading":116,"summary":117,"follow_up":118,"word_count":119,"commitments":120,"compensation":121,"drugs_mentioned":122},"This is an interventional study planning to enroll 100 participants. It compares injecting Mesenchymal Stem Cells into the ACL graft to a sham procedure (a small incision where bone marrow would have been taken).","completed","Biologic Augmentation for ACL Reconstruction","This study is looking at whether adding Mesenchymal Stem Cells (special cells from your own bone marrow) can help heal and integrate the graft used in Anterior Cruciate Ligament (ACL) reconstruction surgery. You might be able to join if you are between 18 and 60 years old, speak English, and are having ACL reconstruction for a recent injury (within 6 months) using a patellar tendon allograft (tissue from a donor). Researchers will measure how well the graft is healing and integrating using MRI scans at 9 months after surgery. They will also look at your reported outcomes and how well your knee functions. The current status of this study is unclear, and it plans to enroll 100 participants.","The primary endpoint is measured at 9 months, suggesting follow-up for at least that long after surgery.",118,"Not specified in the trial record.","Not stated in the trial record.",[],"v2"]