[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"medial-patellofemoral-ligament-reconstruction\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:medial-patellofemoral-ligament-reconstruction":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100561456","phase-4-anterior-femoral-and-adductor-canal-nerve-blocks-in-peds-knees-100561456",false,"NCT06590402","Anterior Femoral and Adductor Canal Nerve Blocks in Peds Knees","A Pilot Study Comparing Anterior Femoral Cutaneous Nerve Blocks to Adductor Canal Blocks in Pediatric Ambulatory Knee Surgeries","Inclusion Criteria:\n\n* 8-18 years old at the time of surgery\n* Patients 40kg and above\n* ACL reconstruction of MPFL reconstruction surgery with participating surgeons\n\nExclusion Criteria:\n\n* revision surgery\n* bilateral surgery\n* general anesthesia\n* contraindications to any part of the study protocol\n* relevant pre-existing neurological deficit\n* chronic pain",true,"ALL","8 Years","18 Years",{"count":21,"type":22},60,"ESTIMATED","INTERVENTIONAL",[25],"PHASE4","The goal of this pilot clinical trial is to compare anterior femoral cutaneous nerve block (AFCN) to adductor canal block ACB) for pediatric patients undergoing either anterior cruciate ligament (ACL) or medial patellofemoral ligament (MPFL). The aims of this trial are:\n\n* To measure postoperative functional outcomes in patients who received AFCNB vs. ACB.\n* To calculate postoperative opioid requirements in pediatric knee surgeries that received AFCNB vs. ACB.\n* To calculate pain intensity levels at rest and with ambulation in patients who received AFCNB vs. ACB.\n* To quantify sensory deficits in patients who received AFCNB vs. ACB.\n* To assess patient-reported outcome measures (e.g., pain expectation scale, pain management satisfaction, PROMIS Pediatric Short Form v1.0 - Physical Activity, PROMIS Scale v1.2 - Global Health) in patients 8-18 years of age who received AFCNB vs. ACB.\n\nSubjects undergoing ACL procedures will be compared between those who received the adductor canal block to those who received the anterior femoral cutaneous nerve block. The researchers will also compare individuals who underwent MPFL procedures and received an anterior femoral cutaneous nerve block with those who received the adductor canal block.\n\nParticipants will:\n\n* Be randomized to receive either the AFCNB or ACB in addition to standard of care analgesia.\n* Maintain a patient diary to document daily pain meds\u002Fpain scores\n* Complete follow up surveys\u002Fquestionnaires via telephone and during their office visits with surgeons.",[28,29],"Anterior Cruciate Ligament Reconstruction","Medial Patellofemoral Ligament Reconstruction","RECRUITING","2025-10-01",{"date":33,"type":34},"2025-10-06","ACTUAL",{"date":36,"type":34},"2025-06-06",{"date":38,"type":22},"2028-01",{"name":40,"class":41},"Hospital for Special Surgery, New York","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":17,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":23,"phases":55,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":42},"100497576","should-you-transfer-the-tubercle-100497576","NCT05759039","SHould You TransFer the Tubercle?","A Randomized Clinical Pilot Trial Comparing Isolated Medial Patellofemoral Ligament Reconstruction to Medial Patellofemoral Ligament Reconstruction Combined with Tibial Tubercle Osteotomy: SHould You TransFer the Tubercle (SHYFT)?","SHYFT","Inclusion Criteria:\n\n* Age 13-30 years\n* Symptomatic recurrent lateral patellofemoral instability\n* TT-TG ≥15mm measured on MRI or ≥18mm on CT scan\n* Closed physes (confirmed on knee x-rays)\n\nExclusion Criteria:\n\n* Caton-Deschamps ratio ≥ 1.4 on lateral radiographs\n* Femoral anteversion ≥ 25 degrees on diagnostic imaging rotational profile\n* Tibial external rotation ≥ 45 degrees on diagnostic imaging rotational profile\n* High-grade trochlear dysplasia requiring trochleoplasty\n* Significant osteoarthritis on skyline plain imaging (Kellgren Lawrence grade ≥ 2)\n* A chondral lesion of the patellofemoral joint that is undergoing a cartilage restoration procedure.\n* Unable to complete computer-based outcome questionnaires\n* Pregnant (at time of surgery)","13 Years","30 Years",{"count":54,"type":22},32,[56],"NA","The aim of this study is to investigate the role of tibial tubercle osteotomy (TTO) on the subjective and objective outcomes following medial patellofemoral ligament reconstruction (MPFL-R) in patients with an increased tibial tubercle-trochlear groove (TT-TG) distance with or without patella alta.\n\nThis Pilot RCT will assess the feasibility of conducting this study for:\n\n1. The ability to recruit study patients\n2. Adherence to the study protocol\n3. Completion rates of patient follow-up at a minimum of 12 months post-operative",[59,60,29],"Patellofemoral Dislocation","Tibial Tubercle Osteotomy","2025-01-31",{"date":63,"type":34},"2025-02-04",{"date":65,"type":34},"2023-09-01",{"date":67,"type":22},"2026-09-01",{"name":69,"class":41},"Banff Sport Medicine Foundation"]