[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"acetabular-fractures\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:acetabular-fractures":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100651784","pericapsular-nerve-group-peng-block-on-postoperative-pain-management-after-acetabular-fracture-fixation-100651784",false,"NCT07765095","Pericapsular Nerve Group (PENG) Block on Postoperative Pain Management After Acetabular Fracture Fixation","Efficacy of Pericapsular Nerve Group (PENG) Block on Postoperative Pain Management After Acetabular Fracture Fixation: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Patient age 18 years or older\n* Acetabular Fracture amenable to surgery through the Kocher-Langenbeck approach\n* Full weight-bearing capacity prior to the trauma\n* Providing written informed consent\n\nExclusion Criteria:\n\n* Age less than 18 years old\n* Fracture pattern not amenable to surgery through Kocher-Langenbeck approach\n* Lower extremity fracture ipsilateral to the acetabular fracture\n* Any traumatic injury that requires surgical management by other surgical specialty\n* Bilateral Acetabular Fractures\n* Limited weight bearing capacity prior to the trauma\n* Procedure performed under any anesthesia other than GETA\n* Chronic opioid use\n* History of Substance Abuse\n* Allergies or history of adverse reactions to any of the drugs used in the\n* Mental Disability\n* History of Psychiatric disorders","ALL","18 Years",{"count":19,"type":20},70,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to find out whether a Pericapsular Nerve Group (PENG) block, a type of nerve block used to control pain, can reduce pain after surgery in adults with an acetabular (hip socket) fracture who are undergoing surgical repair. The study will also evaluate the safety of the PENG block.\n\nThe main questions this study aims to answer are:\n\nDoes a PENG block reduce pain after surgery? Does a PENG block reduce the need for opioid pain medications after surgery? Are there any side effects or complications related to the PENG block? Researchers will compare patients who receive a PENG block with patients who do not receive a PENG block to determine whether the block improves pain control after surgery.\n\nParticipants will:\n\nBe randomly assigned to receive either a PENG block or no PENG block before surgery while under general anesthesia.\n\nUndergo surgery to repair their acetabular fracture. Receive the same standard pain medications after surgery. Be asked to rate their pain at several time points after surgery using a standard pain scale.\n\nHave their use of pain medications, recovery, and any side effects recorded during their hospital stay and follow-up.",[26],"Acetabular Fractures",[26,28,29,30,31],"Pain Management","Pericapsular Nerve Group (PENG)","Open Reduction and Internal Fixation (ORIF)","Regional Block","RECRUITING","2026-08-12",{"date":35,"type":36},"2026-08-14","ACTUAL",{"date":38,"type":36},"2025-09-08",{"date":40,"type":20},"2027-03-30",{"name":42,"class":43},"University of Puerto Rico","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":56,"conditions":57,"keywords":62,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":44},"100598499","relieved-regional-anesthesia-pelvic-fractures-study-study-regional-anesthesia-ra-techniques-for-pain-management-in-pelvic-fractures-a-prospective-monocentric-pilot-cohort-study-100598499","NCT07072286","RELIEVED (REgionaL anesthesIa PElVic fracturEs stuDy) Study. Regional Anesthesia (RA) Techniques for Pain Management in Pelvic Fractures: A Prospective, Monocentric, Pilot Cohort Study.","RELIEVED (REgionaL anesthesIa PElVic fracturEs stuDy) Study. Regional Anesthesia (RA) Techniques for Pain Management in Pelvic Fractures: A Prospective, Monocentric, Pilot Cohort Study. Pain Management in Surgical and Conservative Settings.\"","RELIEVED","Inclusion Criteria:\n\n* Age ≥ 18 years and ability to provide informed consent\n* Patients with pelvic\u002Facetabular fractures requiring surgery\n\nExclusion Criteria\n\n* Age \\\u003C 18 years\n* Absolute contraindications to ALR techniques (uncorrectable coagulopathies, known allergy to local anesthetics, technical impossibility of execution)",{"count":54,"type":20},200,"OBSERVATIONAL","The goal of this observational clinical trial is to assess the impact of Regional Anesthesia (RA) techniques with the strongest anatomical and scientific support in controlling acute post-operative pain in pelvic\u002Facetabular fractures, as well as their potential role in reducing complications related to excessive intra- and postoperative opioid use.\n\nThe main questions it aims to answer are:\n\nDoes RA lower opioid use in the first 24 hours after pelvic\u002Facetabular fractures surgery? Does RA lower pain scores in the first 48 hours after surgery, incidence of complications and occurrence of persistent post-surgical pain?\n\nDuring the hours and days following surgery, the research team will evaluate and assess the intensity of any postoperative pain at predefined time points; quantify the use of pain medications and any related complications; and measure the possible onset of chronic pain and the timeline of functional recovery (through scheduled clinical follow-up at 30, 60, and 90 days).\n\nParticipants will:\n\nat the time of surgery, and only in the presence of trained and certified anesthesiologists, patients will receive regional anesthesia techniques in addition to the standard multimodal analgesic treatment. In the absence of certified anesthesiologists, patients will be treated exclusively with systemic multimodal analgesia according to the standard protocol.\n\nAll the procedures are part of the current clinical practice and no experimental techniques or medications are involved.",[58,59,26,60,61],"Pelvic Bone Injury","Pelvis Injury","Acetabular Surgery","Trauma Injury",[63,64,65,66,67],"regional anethesia","pain management","pelvic fractures","acetabular fractures","surgery","2025-07-09",{"date":70,"type":36},"2025-07-18",{"date":72,"type":36},"2024-07-25",{"date":74,"type":20},"2026-09-25",{"name":76,"class":43},"A.O.U. Città della Salute e della Scienza"]