[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"tha\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:tha":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,53,73,91,121],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":36,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100626579","binaural-beats-for-postoperative-pain-and-anxiety-reduction-100626579",false,"NCT07437469","Binaural Beats for Postoperative Pain and Anxiety Reduction","Binaural Beats vs Music of Choice for Early Postoperative Pain After Ambulatory Total Knee and Total Hip Arthroplasty: A Randomized Controlled Trial","Inclusion Criteria:\n\n* American Society of Anesthesiologists Physical Status Classification System (ASA) 1-3\n* Spinal anesthesia\n* Patients receiving nerve-block in Post-Anesthesia Care Unit (PACU)\n* Primary total hip or total knee arthroplasty\n\nExclusion Criteria:\n\n* Moderate-severe hearing impairment or use of hearing aids\n* History of significant tinnitus, active delirium, chronic high-dose opioid therapy (\\>60 MME\u002Fday baseline)\n* Major psychiatric pathology\n* General anesthesia","ALL","18 Years","99 Years",{"count":20,"type":21},50,"ESTIMATED","INTERVENTIONAL",[24],"NA","To deliver a 30-minute binaural beats audio intervention in PACU and collect pain and anxiety outcomes immediately following surgery, and 4 hours following surgery completion in adults undergoing ambulatory total knee arthroplasty and total hip arthroplasty (TKA and THA).",[27,28,29,30,31,32,33,34,35],"TKA","THA","Anxiety","Binaural Beats","Music Exposure","Total Hip Arthroplasty (THA)","Total Knee Arthroplasty","Total Knee Replacement","Total Hip Replacement",[28,27,37,38,29,39,30,31],"Total hip arthroplasty","Total knee arthroplasty","Pain","RECRUITING","2026-04-29",{"date":43,"type":44},"2026-04-30","ACTUAL",{"date":46,"type":44},"2026-03-09",{"date":48,"type":21},"2026-08-30",{"name":50,"class":51},"University of Miami","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":22,"phases":62,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":52},"100579957","bikini-vs-longitudinal-incision-in-direct-anterior-approach-daa-total-hip-arthroplasty-tha-100579957","NCT06831045","Bikini vs Longitudinal Incision in Direct Anterior Approach (DAA) Total Hip Arthroplasty (THA)","A Clinical Comparison in Wound Healing of Bikini Versus Longitudinal Incision in Direct Anterior Approach Total Hip Arthroplasty in the Obese Patient Population: A Randomized Control Trial","Inclusion Criteria:\n\n* Patients with body mass index greater than or equal to 30\n* Patients undergoing primary unilateral DAA THA\n* Patients undergoing primary THA\n\nExclusion Criteria:\n\n* Patients with body mass index less than 30\n* Patients with a history of prior open surgery on the affected hip\n* Patients unable\u002Funwilling to undergo spinal anesthesia under monitored anesthesia care (MAC)\n* Patients with allergies or absolute contraindication to standardized drugs administered within the University of Miami protocol for total hip replacement\n* The following groups will not be included: adults unable to consent, individuals who are not yet adults, pregnant women, prisoners.",{"count":61,"type":21},110,[24],"The study team is conducting this study to see if there is a difference between the wound healing and participant satisfaction rates between two incision types used during a THA done via the DAA technique.",[28],"2026-03-17",{"date":67,"type":44},"2026-03-18",{"date":69,"type":44},"2025-03-01",{"date":71,"type":21},"2028-04-01",{"name":50,"class":51},{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":22,"phases":82,"briefSummary":84,"conditions":85,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":86,"startDateStruct":87,"completionDateStruct":88,"leadSponsor":90,"locationsCount":52},"100578174","phase-4-duloxetine-for-perioperative-pain-in-hip-arthroplasty-a-rct-100578174","NCT06807866","Duloxetine for Perioperative Pain in Hip Arthroplasty: A RCT","Use of Duloxetine for Perioperative Pain Control After Total Hip Arthroplasty: Randomized Controlled Clinical Trial (RCT)","Inclusion Criteria:\n\n* Patients \\> 18 years of age\n* Patients undergoing primary total hip arthroplasty\n* Ambulatory patient prior to fracture\n* Subjects must be capable of providing informed consent\n* English or Spanish speaking\n\nExclusion Criteria:\n\n* Previous hemiarthroplasty or THA on ipsilateral hip\n* History of Complex Regional Pain Syndrome in ipsilateral extremity\n* History of demyelinating disorder or neurologic deficit that may contribute to altered pain tolerance or sensation\n* Acute or chronic hip infection in ipsilateral extremity\n* Pregnant or breastfeeding\n* Open fracture\n* Polytrauma\n* Intravenous or drug users within 6 months of surgery\n* Liver Failure via clinical diagnosis or international normalized ratio greater than 1.5 or partial thromboplastin time greater than 40\n* Patients on selective serotonin reuptake inhibitor, serotonin norepinephrine reuptake inhibitor, monoamine oxidase inhibitor, and\u002For tricyclic anti-depressant\n* Severe renal dysfunctions, such as glomerular filtration rate less than 30\n* Moderate to severe depression as diagnosed by a clinician\n* Taking cytochrome P450 1A2 inhibitors and cytochrome P450 1A6 inhibitors for the duration of 5 half-lives as these drugs are clinically eliminated within 5 half-lives\n* History of uncontrolled narrow angle glaucoma",{"count":81,"type":21},64,[83],"PHASE4","The primary objective of this study is to compare total narcotic intake standardized via milligram morphine equivalents between duloxetine and placebo cohorts after a total hip arthroplasty.",[28],{"date":67,"type":44},{"date":69,"type":44},{"date":89,"type":21},"2026-12-01",{"name":50,"class":51},{"id":92,"slug":93,"hasResults":11,"nctId":94,"briefTitle":95,"officialTitle":96,"acronym":4,"eligibilityCriteria":97,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":98,"enrollmentInfo":99,"targetDuration":101,"studyType":102,"phases":4,"briefSummary":103,"conditions":104,"keywords":106,"overallStatus":111,"whyStopped":4,"lastUpdateSubmitDate":112,"lastUpdatePostDateStruct":113,"startDateStruct":115,"completionDateStruct":117,"leadSponsor":119,"locationsCount":52},"100622317","a-prospective-multicenter-clinical-study-on-the-efficacy-and-safety-of-the-zirconia-ceramic-hip-joint-prosthesis-system-after-its-market-launch-100622317","NCT07382050","A Prospective Multicenter Clinical Study on the Efficacy and Safety of the Zirconia Ceramic Hip Joint Prosthesis System After Its Market Launch","A Prospective Multicenter Clinical Study on the Efficacy and Safety of the Zirconia Ceramic Hip Joint Prosthesis System After Its Market launchM20251018","Inclusion Criteria:\n\n1. The patient's age ranges from 18 to 80 years old (inclusive), with no gender restrictions.\n2. The patient's bones have matured.\n3. The patient is indicated for hip replacement surgery\n4. The subjects participating in the study were undergoing hip replacement for the first time\n5. The subject or his\u002Fher guardian is willing and able to sign the informed consent form\n\nExclusion Criteria:\n\n1. There are contraindications for hip replacement surgery\n2. It is known that the patient has a history of allergy to one or more implant materials\n3. Pregnant or lactating women\n4. Hip dysplasia is classified into CROWE grades 3 and 4\n5. Those who are physically weak or unable to tolerate surgery due to other systemic diseases, as well as those with an expected lifespan of less than two years\n6. The reasons why other researchers believe that patients are not suitable for this study","80 Years",{"count":100,"type":21},290,"12 Months","OBSERVATIONAL","This study adopted a prospective, multi-center, single-group target value trial design to evaluate the safety and efficacy of the hip joint prosthesis system produced by Beijing Anshou Technology Co., Ltd. in total hip arthroplasty. This clinical study selected seven clinical centers and recruited 290 subjects. Each center competed for enrollment, with the requirement that each center should undertake no less than 8 cases and no more than half of the total cases. The enrollment stopped when the total number of cases met the design requirements. After the patients signed the informed consent form, they entered the screening process. After the screening was successful, the hip joint prosthesis system produced by Beijing Anshou Technology Co., Ltd. was implanted, and follow-up was conducted for the patients at \"before surgery, on the day of surgery, immediately after surgery until discharge, 2 weeks after surgery, 6 weeks after surgery, 3 months after surgery, 6 months after surgery, and 12 months after surgery.\" The demographic information and various evaluation indicators of the subjects were collected.",[28,105],"Prosthesis",[107,108,109,110],"total hip arthroplasty","Zirconia ceramic prosthesis","efficacy","safety","NOT_YET_RECRUITING","2026-01-25",{"date":114,"type":44},"2026-02-02",{"date":116,"type":21},"2026-01-01",{"date":118,"type":21},"2027-12-31",{"name":120,"class":51},"Peking University Third Hospital",{"id":122,"slug":123,"hasResults":11,"nctId":124,"briefTitle":125,"officialTitle":126,"acronym":4,"eligibilityCriteria":127,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":128,"targetDuration":4,"studyType":22,"phases":130,"briefSummary":131,"conditions":132,"keywords":4,"overallStatus":111,"whyStopped":4,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":138,"completionDateStruct":140,"leadSponsor":142,"locationsCount":4},"100565219","the-q-reduce-study-100565219","NCT06639334","The Q-REDUCE Study","A Quick Pathway for Patients With High pRobability of dislocatEd Hemi- or Total Hip Arthroplasty to Minimize the Time From Hospital aDmission to redUCtion of the prosthEsis","Inclusion Criteria:\n\n* a history of either a THA or a HA in combination with at least one of the following terms\n* having sustained a sudden, incorrect movement or twist in the hip joint in either a bending, sitting or supine position leading to inability to stand or walk\n* misalignment of the concerned lower extremity (typically shortened, with inward\u002Foutward rotation)\n\nExclusion Criteria:\n\n* recurrent dislocations during the same hospital admission (already \"in the house\")\n* anticipated difficult airway by the attending anesthesiologist\n* anticipated need for extended respiratory or hemodynamic monitoring by the attending anesthesiologist\n* American Society of Anesthesiologists (ASA) score \\> 3\n* Body Mass Index (BMI) \\> 40\n* active drug abuse\n* contraindication for Propofol or Esketamine",{"count":129,"type":21},120,[24],"The purpose of this study is to design a fast-track pathway for patients referred to the University Hospital of Southern Denmark, Esbjerg, with high probability of having a dislocated hip prosthesis with the primary aim to reduce the time from arrival to reduction and the total hospitalization time. Secondary aims are to\n\n* investigate whether quicker prosthesis reduction influences on hip function and quality of life afterwards\n* reduce the pain experience immediately and in the long term\n* increase patient satisfaction\n\nwithout changing the overall complication rate and readmission\u002Fmortality",[28,133,134],"Dislocation, Hip","PROM","2024-10-10",{"date":137,"type":44},"2024-10-15",{"date":139,"type":21},"2024-11-01",{"date":141,"type":21},"2027-08-31",{"name":143,"class":51},"University of Southern Denmark"]