[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"total-joint-arthroplasty\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:total-joint-arthroplasty":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,38,67,94],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":26,"lastUpdatePostDateStruct":27,"startDateStruct":30,"completionDateStruct":32,"leadSponsor":34,"locationsCount":37},"100385129","total-joint-arthroplasty-in-a-pediatric-population-100385129",false,"NCT04294693","Total Joint Arthroplasty in a Pediatric Population","Inclusion Criteria: Populations 1,2,3\n\n* Age between 10 years and 25 years\n* Undergoing or have undergone total joint arthroplasty at Children's Hospital Colorado for non-solid tumor related reasons\n* Treated at Children's Hospital Colorado by Dr. Nathan Donaldson, DO or Dr. Steven Thorpe, MD or previously by Travis Heare, MD\n\nExclusion Criteria: Populations 1,2,3\n\n* Subjects and\u002For parents not capable of completing basic questionnaires in English (HRQL data will not be collected from non-English speaking subjects because we do not have access to versions of these questionnaires that have been validated in languages other than English. These patients may be included at a later date when validated questionnaires are available).\n* Subjects who underwent hemiarthroplasties, failed rotationplasty to arthroplasty conversions, or joint arthroplasty directly related to a tumor at the location of the joint\n* Subjects diagnosed with mucopolysaccharidoses (MPS), pseudorheumatoid chondrodysplasia, or diastrophic dwarfism\n\nInclusion Criteria: Population 4\n\n* Age between 10 years and 25 years\n* Treated at Children's Hospital Colorado by Dr. Nathan Donaldson, DO, or Dr. Steven Thorpe, MD or previously by Travis Heare, MD\n* Symptomatic joint pain treated non-invasively via lifestyle modifications, over the counter or prescription pain medication, nerve blocks or steroid injections, and\u002For physical therapy\n* Symptomatic joint pain treated via core decompression surgery at Children's Hospital Colorado by Dr. Nathan Donaldson, DO, or Dr. Steven Thorpe, MD, or previously by Travis Heare, MD\n\nExclusion Criteria: Population 4\n\n* Patients who underwent a joint arthroplasty directly related to a tumor at the location of the joint at Children's Hospital Colorado. Patients undergoing or have undergone total joint arthroplasty at Children's Hospital Colorado for non-solid tumor related reasons\n* Subjects diagnosed with mucopolysaccharidoses (MPS), pseudorheumatoid chondrodysplasia, or diastrophic dwarfism","ALL","10 Years","25 Years",{"count":19,"type":20},1000,"ESTIMATED","OBSERVATIONAL","The primary purpose of this study is to examine the functional ability and quality of life in those patients who received a total joint arthroplasty (TJA) for reasons other than having a solid tumor at the location of the joint.",[24],"Total Joint Arthroplasty","RECRUITING","2026-04-16",{"date":28,"type":29},"2026-04-20","ACTUAL",{"date":31,"type":29},"2019-06-03",{"date":33,"type":20},"2061-03",{"name":35,"class":36},"University of Colorado, Denver","OTHER",1,{"id":39,"slug":40,"hasResults":11,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":44,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":15,"minAge":46,"maxAge":47,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":66},"100505187","is-physical-therapy-clearance-before-arthroplasty-home-discharge-necessary-100505187","NCT05858086","Is Physical Therapy Clearance Before Arthroplasty Home Discharge Necessary?","Is Postoperative Physical Therapy Clearance Necessary for Safe Home Discharge After Total Joint Arthroplasty?","PTClearSHoT","Inclusion Criteria:\n\n* are 18 years of age or older\n* undergo primary THA or TKA\n* are eligible for same-day home discharge (friends or family available to stay at home with the patient for one week postoperatively and medically stable for discharge from PACU per anesthesia).\n\nExclusion Criteria:\n\n* 90 years of age or older\n* have sleep apnea (not eligible for same-day discharge)\n* require overnight stay for any reason\n* undergo revision THA or TKA.","18 Years","90 Years",{"count":49,"type":20},210,"INTERVENTIONAL",[52],"NA","Conventionally, physical therapy (PT) clearance is sought before total joint arthroplasty (TJA) discharge. However, PT staffing limitations may preclude same-day discharge in patients having surgery late in the day. Failed same-day discharge in eligible TJA patients results in unnecessary hospital bed occupancy, which increases costs, limits operating room throughput for patients requiring inpatient admission, and introduces risks associated with longer length-of-stay.\n\nIn collaboration with an institutional PT department, the investigators developed a protocol for discharging same-day TJA patients without postoperative PT clearance. Immediately preoperatively, PT administers gait training. Patients are then discharged home after ambulating with post-anesthesia care unit (PACU) nurses trained by PT on postoperative mobilization. This allows for the maximum number of patients discharged home, including the last patient of the day, PT staffing limitations notwithstanding. Single-institution pilot data demonstrates no increased risk of falls, emergency room (ER) visits, or readmissions with this process.\n\nThe investigators propose a prospective, controlled, multicenter study to expand on pilot data. The study aim is to assess safety of day-of-surgery preoperative PT and postoperative ambulation with PACU nursing before TJA discharge. The primary endpoint is postoperative falls, while secondary endpoints include 90-day ER visits, 90-day hospital readmissions, patient-reported outcome measures, and patient satisfaction scores.",[55,24,56],"Physical Therapy","Same-day Discharge","2026-02-06",{"date":59,"type":29},"2026-02-10",{"date":61,"type":29},"2024-09-27",{"date":63,"type":20},"2027-12",{"name":65,"class":36},"University of Maryland, Baltimore",2,{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":15,"minAge":46,"maxAge":4,"enrollmentInfo":74,"targetDuration":4,"studyType":50,"phases":76,"briefSummary":77,"conditions":78,"keywords":79,"overallStatus":84,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":37},"100607876","the-effect-of-guided-imagery-technique-on-anxiety-pain-and-analgesic-use-in-total-joint-arthroplasty-patients-100607876","NCT07194252","The Effect of Guided Imagery Technique on Anxiety, Pain, and Analgesic Use in Total Joint Arthroplasty Patients","The Effect of Guided Imagery Applied Before and After Surgery on Surgical Anxiety, Pain, and Analgesic Consumption in Patients Undergoing Total Joint Arthroplasty: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients who have undergone unilateral arthroplasty surgery,\n* Without cognitive impairment,\n* Who speak and write Turkish,\n* Without hearing or vision problems,\n* Without any other acute illness causing pain or anxiety,\n* Who received the same analgesic agent in the treatment protocol during the postoperative period,\n* And who volunteered to participate in the study will be included.\n\nExclusion Criteria:\n\n* Having a diagnosis of chronic pain syndrome or neuropathic pain,\n* Having a diagnosis of psychiatric illness\u002Fbeing under treatment\n* Continuous use of analgesic\u002Fsedative medication that may affect the pain threshold,\n* Hearing impairment or severe cognitive impairment that prevents participation in guided imagery applications.",{"count":75,"type":20},128,[52],"This randomized controlled study will investigate the effects of guided imagery on preoperative anxiety and postoperative pain and analgesic consumption in patients undergoing total joint arthroplasty. Conducted between September 2025 and June 2026 at a public hospital in Zonguldak, Turkey, the study will include patients scheduled for total joint arthroplasty following ethics committee approval. The intervention group will receive guided imagery twice preoperatively and once daily at 48 and 72 hours postoperatively. Outcomes will be assessed using the Surgical Anxiety Scale, surgery-specific anxiety scale, Numerical Rating Scale (NRS), and analgesic consumption tracking.",[24],[80,81,82,83],"pain","anxiety","analgesic","total joint arthroplasty","NOT_YET_RECRUITING","2025-09-18",{"date":87,"type":29},"2025-09-26",{"date":89,"type":20},"2025-09-22",{"date":91,"type":20},"2026-06-22",{"name":93,"class":36},"Ankara Yildirim Beyazıt University",{"id":95,"slug":96,"hasResults":11,"nctId":97,"briefTitle":98,"officialTitle":99,"acronym":100,"eligibilityCriteria":101,"healthyVolunteers":102,"sex":15,"minAge":46,"maxAge":103,"enrollmentInfo":104,"targetDuration":4,"studyType":50,"phases":106,"briefSummary":107,"conditions":108,"keywords":111,"overallStatus":84,"whyStopped":4,"lastUpdateSubmitDate":115,"lastUpdatePostDateStruct":116,"startDateStruct":118,"completionDateStruct":120,"leadSponsor":122,"locationsCount":4},"100552025","clinical-efficacy-of-self-adhesive-silicone-gel-waterproof-dressings-versus-conventional-dressings-in-the-healing-of-incisions-after-total-joint-arthroplasty-100552025","NCT06467721","Clinical Efficacy of Self-adhesive Silicone Gel Waterproof Dressings Versus Conventional Dressings in the Healing of Incisions After Total Joint Arthroplasty","Clinical Efficacy of Self-adhesive Silicone Gel Waterproof Dressings Versus Conventional Dressings in the Healing of Incisions After Total Joint Arthroplasty: a Prospective, Randomized Controlled Trial Study","Yes","Inclusion Criteria:\n\n1. Age ≥18 years old, gender is not limited;\n2. Meet the diagnostic criteria for artificial joint replacement;\n3. Initial joint replacement surgery;\n4. Voluntary and signed informed consent.\n\nExclusion Criteria:\n\n1. Allergic to self-adhesive silicone rubber waterproof dressing;\n2. Patients with severe knee joint infection who cannot undergo artificial joint replacement;\n3. Progressive renal insufficiency (stage 4 and above) or glomerular filtration rate less than 30ml\u002Fmin;\n4. periprosthesis infection after multiple joint replacement;\n5. Active infection at the site of intravenous or joint injection;\n6. long-term use of anticoagulants or antiplatelet drugs due to other diseases;\n7. Have sepsis or positive blood culture within the last 30 days;\n8. Radiotherapy and chemotherapy are required due to neoplastic diseases;\n9. Receiving systemic glucocorticoid therapy (prednisone \\> 10mg\u002F day or equivalent hormone medication);\n10. severe immunodeficiency diseases (such as stage 3 HIV, sickle cell anemia, splenectomy, etc.);\n11. Have a history of drug abuse;\n12. Treatment of bone marrow or other transplants with immunosuppressive drugs;\n13. Pregnant, parturient and lactating women;\n14. Participating in other clinical trials;\n15. Researchers believe that other reasons are not appropriate for clinical trial participants.",true,"80 Years",{"count":105,"type":20},600,[52],"The efficacy of using self-adhesive silicone gel waterproof dressings versus conventional gauze dressings for recovery after total joint arthroplasty (TJA) remains unclear. In our study, we conducted a prospective, randomized controlled trial to compare these two types of dressings. Patients were divided into two groups following TJA, and we collected primary outcome measures such as skin infection rate and re-operation rate. Additionally, we gathered blood inflammatory indicators, including C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR), to evaluate the effectiveness of the two treatments. Finally, we perform one year follow up including REEDA score, MSS score to evaluate the recovery of the skin.",[109,110,24],"Self-adhesive Silicone Gel Waterproof Dressing","Gauze Dressing",[112,113,83,114],"self-adhesive silicone gel waterproof dressing","gauze dressing","RCT","2024-06-15",{"date":117,"type":29},"2024-06-21",{"date":119,"type":20},"2024-08-01",{"date":121,"type":20},"2026-12-31",{"name":123,"class":36},"First Affiliated Hospital of Xinjiang Medical University"]