[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT07708584":3,"trial-entities:NCT07708584":137,"trial-summary:NCT07708584":140},{"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":26,"study_type":29,"primary_purpose":30,"phases":31,"enrollment_info":33,"interventions":36,"primary_outcomes":49,"secondary_outcomes":77,"sex":82,"minimum_age":83,"maximum_age":84,"healthy_volunteers":85,"eligibility_criteria":86,"std_ages":102,"locations":105,"central_contacts":129,"overall_officials":134,"references":135,"see_also_links":136},"NCT07708584","2026P000101","Brostrom Chronic Lateral Ankle Instability Repairs Augmented With BioBrace®","The Effect of Augmented Brostrom Repair Using Bioinductive Implant in Patients With Lateral Ankle Instability","RECRUITING","2028-06","2026-07","2026-07-16","2026-06","Massachusetts General Hospital","OTHER",true,"The purpose of this investigation is to evaluate pre- and post-operative patient reported outcomes and functional scores after open non-augmented Broström repair or open Broström repair augmented with the BioBrace Implant.","This is a single-center, prospective, randomized (1:1) interventional study investigating the use of the BioBrace® Implant in lateral ankle ligament repair procedures performed using the Broström technique. Eligible participants who meet study criteria will be enrolled and randomized into one of two study arms:\n\nControl Group: Open standard Broström repair of the lateral ankle\n\nTreatment Group: Open Broström repair of the lateral ankle using a suture-anchor construct augmented with the BioBrace® Implant.\n\nBoth groups will be immobilized for 2 weeks and then will undergo standard accelerated rehabilitation protocols (early weight-bearing and sport-specific training) unless they are not tolerated which will lead to using traditional standard protocols.\n\nClinical evaluations will be conducted at baseline (preoperatively), and postoperatively at 2 weeks, 2 months, 6 months, and 12 months using various patient-reported outcome measures to asses pain, function, satisfaction, activity and safety post surgery. Participants will also receive biweekly (every 2 weeks) electronic questionnaires assessing return to sport and return to daily\u002Frecreational activity. These biweekly assessments will continue until the participant reports full return to their preoperative level of activity or sport. Participants who do not reach preoperative activity\u002Fsport level will continue receiving biweekly questionnaires through the 1 year final visit.",[19,20,21,22,23,24,25],"Lateral Ankle Instability","Chronic Lateral Ankle Instability","Brostrom Procedure","ATFL","Anterior Talofibular Ligament","Ankle","Bioinductive Implant",[19,27,25,22,23,21,28,24],"Brostrom Repair","Ankle Surgery","INTERVENTIONAL","TREATMENT",[32],"NA",{"count":34,"type":35},75,"ESTIMATED",[37,43],{"type":38,"name":39,"description":40,"armGroupLabels":41},"PROCEDURE","Standard Brostrom Repair","Standard-of-care Brostrom repair for chronic lateral ankle instability",[42],"Standard Brostrom Repair (SBR)",{"type":44,"name":45,"description":46,"armGroupLabels":47},"DEVICE","Brostrom repair with augmentation","Brostrom repair with BioBrace",[48],"Augmented Brostrom Repair (ABR)",[50,54,58,61,64,67,70,74],{"measure":51,"description":52,"timeFrame":53},"Pain VAS","The pain VAS (Visual Analog Scale) is a unidimensional measure of pain intensity, used to record patients' pain progression, or compare pain severity between patients. It consists of a line marked from 0 to 10, with 0 representing \"no pain\" at one end and 10 \"worst imaginable pain\" at the other; patients mark their pain level on the line, which is then measured to provide a numerical score from 0 to 10.","From enrollment to the last follow-up at 12 months",{"measure":55,"description":56,"timeFrame":57},"PROMIS Scale v2.0 - Pain Intensity 3a","The PROMIS Scale v2.0 - Pain Intensity 3a scale utilizes a 3-question questionnaire to assess patients' pain experiences over the previous 7 days. The items include the intensity of pain at its worst, the intensity of pain on average, and the level of pain right now. The items are scored on a scale from \"Had no pain\" to \"Very severe\".","From enrollment to the last follow-up at 12 months.",{"measure":59,"description":60,"timeFrame":57},"NIH Toolbox Pain Interference CAT Ages 18 v3.0","The NIH Toolbox Pain Interference CAT Ages 18 v3.0 is a computerized adaptive test that evaluates how much pain has interfered with and affected a person's life and daily activities over the previous 7 days. The questions are generated dynamically based on previous answers. Results are reported as a T-score. A higher T-score indicates a greater degree of pain interference.",{"measure":62,"description":63,"timeFrame":57},"PROMIS Scale v1.2 - Global Mental 2a","The PROMIS Scale v1.2 - Global Mental 2a is a two-question questionnaire assessing participants' mental health, mood, ability to think, and satisfaction with social activities and relationships. The questions are scored from \"Excellent\" to \"Poor\".",{"measure":65,"description":66,"timeFrame":57},"PROMIS Scale v1.2 - Global Physical 2a","The PROMIS Scale v1.2 - Global Physical 2a is a two-question questionnaire designed to assess a participant's overall physical well-being. The participants are asked to rate their physical health on a scale from \"Excellent\" to \"Poor\" and their ability to carry out physical activities of daily living on a scale from \"Completely\" to \"Not at all\".",{"measure":68,"description":69,"timeFrame":57},"Foot and Ankle Outcome Score (FAOS)","The Foot and Ankle Outcome Score (FAOS) is a 42-item questionnaire with 5 subscales: symptoms (5 items), stiffness (2 items), pain (9 items), daily living (17 items), sports and recreational activities (5 items), and quality of life (4 items). Each question is graded on a 5-point scale (none, mild, moderate, severe, and extreme problems).",{"measure":71,"description":72,"timeFrame":73},"Foot and Ankle Ability Measure Scored","The Foot and Ankle Ability Measure Scored tool has two sections. The first section asks participants to rate their difficulty completing activities of daily living on a scale from \"No difficulty\" to \"Unable to do\" over 21 different questions along with a rating their current level of function from 0 to 100, with 100 being their prior level of function. The second section asks participants to rate their difficulty in participating in sports activities on a scale from \"No difficulty at all\" to \"Unable to do\" over 7 different questions along with a rating their current level of function during sport activities from 0 to 100, with 100 being their prior level of function.","From enrollment to last follow-up at 12 months.",{"measure":75,"description":76,"timeFrame":57},"Clinical Assessment","Clinicians will assess participants during their follow-up appointments. The clinicians will measure an anterior drawer test, range of motion assessment, hindfoot alignment, wound\u002Fincision assessment, complications assessment, and a physical activity assessment.",[78],{"measure":79,"description":80,"timeFrame":81},"Return to Activity","Participants will fill out biweekly (2 weeks) surveys assessing their participation in any physical activities or sport, participation in their primary physical activities or sport, how often and how long they participated, their performance in those activities, and their own subjective understanding of why their performance may be different than before their injuries.","From baseline until participants report full return to activity or until last follow-up at 12 months.","ALL","18 Years","65 Years",false,{"inclusion":87,"exclusion":92,"raw_text":101},[88,89,90,91],"Age 18-65 years","Chronic lateral ankle instability (\\>3 months) confirmed by clinical examination (positive anterior drawer test or talar tilt \\>10°) and imaging (stress X-ray or MRI).","No prior ankle surgery on the affected limb.","Willingness to follow postoperative visits and rehabilitation protocols and filling out the patient reported outcome measures (PROMs) forms.",[93,94,95,96,97,98,99,100],"BMI\\>40","Significant secondary procedures done at the time of repair, including micro-fracture, or any other treatment of osteochondral lesions of the talus or tibia.","Concomitant deltoid ligament insufficiency.","Any worker's compensation case or any subject with a history of infection of the ankle predating the ankle repair. Current orthopedic issues, not related to the ankle, that prevented the patient from performing the functional tests.","Concomitant osteochondral lesions, significant degenerative changes, or severe varus\u002Fvalgus deformity, neuromuscular disorders or non-adherence concerns.","Pregnant","Diagnosis of Ehlers-Danlos Syndrome or other connective tissue \u002F hyperlaxity disorder.","Prior revision ankle ligament surgery on the affected limb (any revision Broström or lateral ligament reconstruction).","Inclusion Criteria:\n\n* Age 18-65 years\n* Chronic lateral ankle instability (\\>3 months) confirmed by clinical examination (positive anterior drawer test or talar tilt \\>10°) and imaging (stress X-ray or MRI).\n* No prior ankle surgery on the affected limb.\n* Willingness to follow postoperative visits and rehabilitation protocols and filling out the patient reported outcome measures (PROMs) forms.\n\nExclusion Criteria:\n\n* BMI\\>40\n* Significant secondary procedures done at the time of repair, including micro-fracture, or any other treatment of osteochondral lesions of the talus or tibia.\n* Concomitant deltoid ligament insufficiency.\n* Any worker's compensation case or any subject with a history of infection of the ankle predating the ankle repair. Current orthopedic issues, not related to the ankle, that prevented the patient from performing the functional tests.\n* Concomitant osteochondral lesions, significant degenerative changes, or severe varus\u002Fvalgus deformity, neuromuscular disorders or non-adherence concerns.\n* Pregnant\n* Diagnosis of Ehlers-Danlos Syndrome or other connective tissue \u002F hyperlaxity disorder.\n* Prior revision ankle ligament surgery on the affected limb (any revision Broström or lateral ligament reconstruction).",[103,104],"ADULT","OLDER_ADULT",[106,120],{"facility":13,"status":8,"city":107,"state":108,"zip":109,"country":110,"contacts":111,"geoPoint":117},"Boston","Massachusetts","02114","United States",[112],{"name":113,"role":114,"phone":115,"email":116},"Gregory Waryasz, MD","CONTACT","781-487-4338","gwaryasz@mgb.org",{"lat":118,"lon":119},42.35843,-71.05977,{"facility":121,"status":8,"city":107,"state":108,"zip":122,"country":110,"contacts":123,"geoPoint":128},"Brigham and Women's Hospital","02115",[124],{"name":125,"role":114,"phone":126,"email":127},"Christopher Miller, MD","617-525-9382","cpmiller@mgb.org",{"lat":118,"lon":119},[130],{"name":131,"role":114,"phone":132,"email":133},"Soheil Ashkani-Esfahani, MD MPH","510-850-6056","sashkaniesfahani@mgh.harvard.edu",[],[],[],{"nct_id":4,"conditions":138,"biomarkers":139},[19],[],{"nct_id":4,"found":15,"summary":141,"prompt_version":150},{"design":142,"status":143,"heading":6,"summary":144,"follow_up":145,"word_count":146,"commitments":147,"compensation":148,"drugs_mentioned":149},"This is a single-center study that will randomly assign 75 participants to one of two treatment groups.","completed","This study is looking at two ways to repair chronic lateral ankle instability (when your ankle frequently gives out or feels loose). One group will receive the standard Brostrom repair surgery. The other group will have the Brostrom repair augmented (strengthened) with a device called BioBrace®. Researchers want to see how well each method helps with pain and ankle function after surgery. You might be able to join if you are between 18 and 65 years old, have had chronic ankle instability for over three months, and haven't had previous ankle surgery on that ankle. The study is currently recruiting participants.","Participants will be followed for 12 months after surgery to assess pain and other outcomes.",101,"You would have surgery, followed by immobilization for two weeks, and then rehabilitation. You would also attend follow-up visits and complete electronic questionnaires for up to 12 months.","Not stated in the trial record.",[39],"v2"]