[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"knee-arthroscopic-surgery\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:knee-arthroscopic-surgery":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,42,69,92],{"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":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100652085","phase-4-effect-of-dexmedetomidine-combined-with-fnbacb-on-sleep-quality-after-knee-surgery-100652085",false,"NCT07767383","Effect of Dexmedetomidine Combined With FNB\u002FACB on Sleep Quality After Knee Surgery","Effect of Dexmedetomidine Combined With FNB\u002FACB on Sleep Quality After Knee Surgery: A Randomized Controlled Factorial Trial","Inclusion Criteria:\n\n1. Age 18 to 85 years.\n2. American Society of Anesthesiologists (ASA) physical status I to III.\n3. Body Mass Index (BMI) between 18 and 30 kg\u002Fm² and body weight \\> 50 kg.\n4. Scheduled for elective knee arthroscopy under general anesthesia.\n5. Complete preoperative workup, confirmed diagnosis, and indication for knee arthroscopy with complete postoperative medical records.\n6. Normal mental and cognitive status.\n7. Patient or legally authorized representative has provided written informed consent for anesthesia and study participation.\n\nExclusion Criteria:\n\n1. Refusal to participate in the study.\n2. Inability to communicate effectively.\n3. Known allergy or contraindication to any study drug (ropivacaine, dexmedetomidine, propofol, sufentanil, remifentanil, vecuronium, or sevoflurane).\n4. History of knee trauma or knee surgery; diagnosed with immune system disorders (e.g., rheumatoid arthritis, systemic lupus erythematosus); neuromuscular diseases or psychiatric disorders; restless legs syndrome (RLS); periodic limb movement disorder (PLMD).\n5. Coagulation disorders or local infection at the puncture site precluding peripheral nerve block.\n6. Severe hepatic or renal dysfunction.\n7. Severe cardiopulmonary insufficiency.\n8. Pregnancy.\n9. Diagnosis of obstructive sleep apnea (OSA) or requirement for continuous positive airway pressure (CPAP) therapy.\n10. Regular use of sedative-hypnotic drugs (benzodiazepines, non-benzodiazepine hypnotics, melatonin receptor agonists, etc.) or antidepressants\u002Fanxiolytics known to affect sleep architecture (e.g., trazodone, mirtazapine) within the past 1 month.\n11. Pittsburgh Sleep Quality Index (PSQI) score \\> 5.",true,"ALL","18 Years","85 Years",{"count":21,"type":22},136,"ESTIMATED","INTERVENTIONAL",[25],"PHASE4","The goal of this randomized, double-blind, placebo-controlled, 2×2 factorial trial is to evaluate the effect of intraoperative dexmedetomidine combined with either femoral nerve block (FNB) or adductor canal block (ACB) on postoperative sleep quality in patients aged 18-85 years with ASA I-III undergoing elective knee arthroscopy under general anesthesia.\n\nThe main questions it aims to answer are:\n\n1. Does intraoperative dexmedetomidine infusion (0.5 μg\u002Fkg\u002Fh) improve postoperative sleep quality as measured by the Pittsburgh Sleep Quality Index (PSQI) at 24 h and 48 h after surgery?\n2. Is there an interaction between the type of nerve block (FNB vs. ACB) and the use of dexmedetomidine on postoperative sleep quality?",[28],"Knee Arthroscopic Surgery","RECRUITING","2026-08-13",{"date":32,"type":33},"2026-08-17","ACTUAL",{"date":35,"type":33},"2026-01-15",{"date":37,"type":22},"2026-12-31",{"name":39,"class":40},"Affiliated Hospital of Nantong University","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":17,"minAge":48,"maxAge":4,"enrollmentInfo":49,"targetDuration":4,"studyType":23,"phases":51,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":41},"100648547","the-effect-of-nutritional-education-on-post-arthroscopic-nutritional-status-100648547","NCT07723742","The Effect of Nutritional Education on Post-Arthroscopic Nutritional Status","Inclusion Criteria:\n\n* aged 10 years and older and scheduled for a knee or shoulder arthroscopic procedure\n\nExclusion Criteria:\n\n* participants not undergoing arthroscopic surgery\n* patients under 10 years of age\n* participants taking appetite-suppressant medications","10 Years",{"count":50,"type":22},200,[52],"NA","The purpose of this study is to determine how patient nutrition effects post-operative outcomes for patients undergoing arthroscopic surgery",[55,56,57,58,28],"Arthroscopic Surgery","Nutrition","Orthopedic Surgery","Shoulder Arthroscopic Surgery","NOT_YET_RECRUITING","2026-07-20",{"date":62,"type":33},"2026-07-23",{"date":64,"type":22},"2026-09",{"date":66,"type":22},"2029-12",{"name":68,"class":40},"University of Alabama at Birmingham",{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":75,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":23,"phases":79,"briefSummary":80,"conditions":81,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":41},"100620492","video-based-education-versus-in-person-education-in-patients-undergoing-arthroscopic-partial-meniscectomy-100620492","NCT07358325","Video-Based Education Versus In-Person Education in Patients Undergoing Arthroscopic Partial Meniscectomy","Effectiveness of a Video-Based Educational Intervention Compared With In-Person Education on Psychosocial and Functional Outcomes in Patients Undergoing Arthroscopic Partial Meniscectomy: A Noninferiority Randomized Controlled Trial","NI-RCT","Inclusion Criteria\n\n* Patients scheduled for arthroscopic partial meniscectomy (medial or lateral meniscus) performed in a day-hospital setting.\n* Traumatic or degenerative meniscal tears.\n* Treatment at the Hip and Knee Orthopedic Unit of the Humanitas Clinical Institute.\n* Age ≥ 18 years.\n* Access to adequate video support.\n* Sufficient proficiency in the Italian language.\n\nExclusion Criteria\n\n* Previous surgery on either knee within the past 5 years.\n* Significant postoperative hematoma requiring aspiration.\n* Neurological conditions potentially affecting functional or motor recovery.\n* Musculoskeletal conditions potentially affecting functional or motor recovery.\n* Rheumatologic conditions potentially affecting functional or motor recovery.\n* Internal medicine conditions potentially affecting functional or motor recovery.\n* Oncological conditions potentially affecting functional or motor recovery.\n* Cognitive or psychiatric disorders (Mini-Mental State Examination ≤ 21).",{"count":78,"type":22},166,[52],"The primary aim of the study is to investigate whether video-based education and exercise-program is non-inferior to in-person instructions in improving pain-related self-efficacy in patients undergoing arthroscopic partial meniscectomy in a day-hospital setting. Secondary aims are to explore the potential superiority of the video-based program compared to in-person instructions in reducing disability and kinesiophobia in the same patient population.",[82,28],"Partial Meniscectomy","2026-02-03",{"date":85,"type":33},"2026-02-05",{"date":87,"type":22},"2026-01-19",{"date":89,"type":22},"2026-06",{"name":91,"class":40},"Istituto Clinico Humanitas",{"id":93,"slug":94,"hasResults":11,"nctId":95,"briefTitle":96,"officialTitle":97,"acronym":4,"eligibilityCriteria":98,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":99,"enrollmentInfo":100,"targetDuration":4,"studyType":23,"phases":102,"briefSummary":103,"conditions":104,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":41},"100596509","tips-block-vs-iv-analgesia-for-postoperative-pain-after-knee-arthroscopy-100596509","NCT07046390","TIPS Block vs. IV Analgesia for Postoperative Pain After Knee Arthroscopy","Comparative Study Between Triple Injection Peri-Sartorius (TIPS) Block Versus Intravenous Analgesia for Postoperative Analgesia After Knee Arthroscopy","Inclusion Criteria:\n\n.Age 18-40 years undergoing knee arthroscopy. .Sex: Both sexes.\n\n.American Society of Anaesthesiologists (ASA) Physical Status Class I and II\n\nExclusion Criteria:\n\n.Declining to give written informed consent. .History of allergy to the medications used in the study. .Contraindications to regional anesthesia (including patient refusal, coagulopathy and local infection).\n\nPsychiatric disorder. .American Society of Anesthesiologists (ASA) Physical Status Class III and IV.\n\n* Patients with body mass index (BMI) \\>35 kg\u002Fm2 .Neurological deficits or mobility-related disorders of the non-operated limb .\n* Moderate to severe hepatic , renal diseases and cardiac disease.","40 Years",{"count":101,"type":22},52,[52],"In this study participants are aiming to compare triple injection peri-sartorius (TIPS) block versus intravenous analgesia for postoperative analgesia after knee arthroscopy regarding efficacy of pain relief and early ambulation",[28,105],"Nerve Block","2025-06-29",{"date":108,"type":33},"2025-07-01",{"date":110,"type":22},"2025-07-20",{"date":112,"type":22},"2026-08-20",{"name":114,"class":40},"Ain Shams University"]