[{"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":75},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"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":19,"type":20},110,"ESTIMATED","INTERVENTIONAL",[23],"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.",[26,27,28],"Prospective","Randomized","Double-blind",[30,31],"Pericapsular Nerve Group Block","hip endoprostheses","RECRUITING","2024-08-13",{"date":35,"type":36},"2024-08-16","ACTUAL",{"date":38,"type":36},"2024-03-07",{"date":40,"type":20},"2025-03",{"name":42,"class":43},"Diakonie-Klinikum Stuttgart","OTHER",1,{"id":46,"slug":4,"hasResults":10,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":51,"sex":16,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":21,"phases":56,"briefSummary":57,"conditions":58,"keywords":59,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":44},"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":55,"type":20},500,[23],"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.",[26],[60,61,62,63,64,65],"Hip arthroplasty","Implant survival","Clinical outcome","X-ray","Implant Migration","Patient reported outcomes","2022-10-03",{"date":68,"type":36},"2022-10-04",{"date":70,"type":36},"2020-08-01",{"date":72,"type":20},"2030-08-01",{"name":74,"class":43},"Sahlgrenska University Hospital",""]