[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"prospective\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:prospective":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100558893","the-analgesic-efficacy-of-pericapsular-nerve-group-peng-block-in-patients-undergoing-primary-total-hip-arthoplasty-100558893",false,"NCT06557044","The Analgesic Efficacy of Pericapsular Nerve Group (PENG) Block in Patients Undergoing Primary Total Hip Arthoplasty:","The Analgesic Efficacy of Pericapsular Nerve Group (PENG) Block in Patients Undergoing Primary Total Hip Arthoplasty: a Prospective, Double-blinded, Randomized Controlled Trial","PENG","Inclusion Criteria:\n\n* planned cementless hip TEP operation for primary coxarthrosis via minimally invasive anterolateral approach using the identical implant system (Taperloc stem, Plamafit cup)\n* Patient capable of giving consent\n* Informed consent has been obtained\n* age \\> 18 years\n\nExclusion Criteria:\n\n* Refusal to participate in the study\n* Regular use of opioids\n* Known chronic pain symptoms\n* Infections in the area of the puncture site\n* Presence of a contraindication to ropivacaine\n* Presence of a contraindication to metamizole\n* Presence of a contraindication to postoperative analgesia with diclofenac\n* Secondary forms of osteoarthritis with deformities (i.e. high-grade dysplasia, secondary conditions after trauma, secondary conditions after childtrauma, secondary conditions after childhood hip joint diseases\n* Spinopelvic dysbalance, spinal canal stenosis\n* Previous operations on the hip\u002Fpelvis","ALL","18 Years",{"count":20,"type":21},110,"ESTIMATED","INTERVENTIONAL",[24],"NA","The aim of this study is to investigate the analgesic efficacy of the pericapsular nerve group (PENG) block during the implantation of hip endoprostheses. The study is designed as a prospective randomized double-blind study and the study participants were randomized into 2 arms and either 20 ml ropivacaine 0.5% (verum group) or 20 ml physiological saline solution (placebo group) will be applied.",[27,28,29],"Prospective","Randomized","Double-blind",[31,32],"Pericapsular Nerve Group Block","hip endoprostheses","RECRUITING","2024-08-13",{"date":36,"type":37},"2024-08-16","ACTUAL",{"date":39,"type":37},"2024-03-07",{"date":41,"type":21},"2025-03",{"name":43,"class":44},"Diakonie-Klinikum Stuttgart","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":17,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":61,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":45},"100389390","a-register-based-prospective-study-during-implementation-of-a-new-cup-100389390","NCT04350255","A Register Based Prospective Study During Implementation of a New Cup","STEISURE - Trident II - A Registerbased Multicentric Prospective Study","Inclusion Criteria:\n\n* Primary hip replacement\n* Eligible for uncemented fixation of the acetabular component\n* Suitable for one of the stem designs from Stryker Orthopaedics\n* Accepts follow-up according to the study protocol\n\nExclusion Criteria:\n\n* Difficulties to understand written information due to language problems or other reasons\n* Use of augments needed\n* Acute hip fracture\n* Tumor in the hip joint",true,"30 Years","75 Years",{"count":57,"type":21},500,[24],"In a prospective register-based study, we aim to evaluate the implant survival, clinical outcomes and X-ray findings by following a cohort of patients operated with the Trident II cup.",[27],[62,63,64,65,66,67],"Hip arthroplasty","Implant survival","Clinical outcome","X-ray","Implant Migration","Patient reported outcomes","2022-10-03",{"date":70,"type":37},"2022-10-04",{"date":72,"type":37},"2020-08-01",{"date":74,"type":21},"2030-08-01",{"name":76,"class":44},"Sahlgrenska University Hospital"]