[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pericapsular-nerve-group-block-peng-block\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pericapsular-nerve-group-block-peng-block":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,77],{"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":32,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":4},"100644066","penglfcn-block-vs-qipb-for-total-hip-arthroplasty-100644066",false,"NCT07667231","PENG+LFCN Block vs QIPB for Total Hip Arthroplasty","Comparison Between Quadro-iliac Plane Block (QIPB) and Pericapsular Nerve Group (PENG) Block Combined With Lateral Femoral Cutaneous Nerve Block for Total Hip Arthroplasty: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Age between 18 and 80 years\n* American Society of Anesthesiologists physical status I-III\n* Scheduled for elective unilateral primary total hip arthroplasty\n* Surgery planned under spinal anesthesia\n* Ability to understand and use the Numeric Rating Scale\n* Written informed consent provided\n\nExclusion Criteria:\n\n* Refusal to participate\n* Revision total hip arthroplasty\n* Bilateral total hip arthroplasty\n* Contraindication to spinal anesthesia\n* Contraindication to peripheral nerve block\n* Known allergy to local anesthetics or study drugs\n* Coagulopathy or anticoagulant use incompatible with neuraxial\u002Fregional anesthesia\n* Infection at the block injection site\n* Pre-existing neurological deficit involving the operative lower extremity\n* Peripheral neuropathy\n* Chronic opioid use\n* Cognitive impairment or inability to communicate reliably\n* Severe hepatic or renal failure\n* Body mass index \\>35 kg\u002Fm²\n* Pregnancy","ALL","18 Years","80 Years",{"count":20,"type":21},60,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized clinical trial aims to evaluate and compare the analgesic efficacy and functional outcomes of the quadro-iliac plane block (QIPB) and the pericapsular nerve group (PENG) block combined with lateral femoral cutaneous nerve(LFCN) block in patients undergoing total hip arthroplasty. The primary outcome is the Numeric Rating Scale (NRS) within the first 48 hours after surgery. Secondary outcomes include postoperative total opioid consumption, ıncidence of quadriceps motor block, time to first ambulation, block performance time, falls, length of hospital stay, block- related complications(hematoma,local anesthetic systemic complications, vascular puncture, and infection), patient satisfaction assessed using a Likert scale, and incidence of postoperative nausea and vomiting.",[27,28,29,30,31],"Quadro-Iliac Plane Block","Pericapsular Nerve Group Block (PENG Block)","Hip Arthroplasty, Total","Pain Management","Lateral Femoral Cutaneous Nerve Block",[33,34,35],"QIPB","PENG","LFCN","NOT_YET_RECRUITING","2026-06-20",{"date":39,"type":40},"2026-06-25","ACTUAL",{"date":42,"type":21},"2026-11-15",{"date":44,"type":21},"2027-09-15",{"name":46,"class":47},"Antalya City Hospital","OTHER",{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":64,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":76},"100640595","ultrasound-guided-peng-block-for-chronic-shoulder-pain-100640595","NCT07607691","Ultrasound-Guided PENG Block for Chronic Shoulder Pain","Evaluation of the Analgesic Efficacy and Functional Outcomes of Ultrasound-Guided PENG Block in Chronic Shoulder Pain","Inclusion Criteria:\n\n* Age 18 years or older.\n* Patients presenting with chronic shoulder pain lasting longer than 3 months.\n* Initial pain intensity score greater than 4 on the Numerical Rating Scale (NRS \\> 4).\n* Patients who have not responded to conservative or medical treatments.\n* Voluntary acceptance of the ultrasound-guided shoulder PENG block treatment and compliance with the scheduled follow-up protocol.\n\nExclusion Criteria:\n\n* Patients currently using anticoagulants or diagnosed with coagulation disorders (bleeding diathesis).\n* Patients with psychomotor or cognitive disorders that prevent cooperative evaluation.\n* Presence of active bacterial infection, open wounds, or infectious discharge at the planned needle injection site.\n* History of shoulder surgery at the intervention site within the last 6 months.\n* Known allergy or hypersensitivity to local anesthetics (lidocaine) or corticosteroids (dexamethasone).\n* Pregnant or breastfeeding patients.\n* Patients who reject the procedure or fail to comply with the scheduled follow-up visits.",{"count":56,"type":21},45,[24],"The purpose of this prospective, observational study is to evaluate the clinical and functional outcomes of ultrasound-guided Pericapsular Nerve Group (PENG) block in patients suffering from chronic shoulder pain. Chronic shoulder pain is a highly prevalent musculoskeletal problem that significantly restricts daily activities and diminishes the patient's quality of life. While conservative treatments and various interventional injections are widely used, long-term efficacy can be limited, and systemic side effects may occur. The shoulder PENG block is a novel regional analgesia technique that specifically targets the articular (sensory) branches of the nerves innervating the shoulder joint capsule without affecting the motor branches. In this single-center study, a total of 45 eligible adult patients with chronic shoulder pain who did not respond to conservative medical treatments will receive an ultrasound-guided PENG block as part of their routine clinical care. The procedure will be performed under sterile conditions using a combination of local anesthetic (lidocaine) and dexamethasone. Patient pain levels will be assessed using the Numerical Rating Scale (NRS), shoulder disability and functional status will be measured using the Shoulder Pain and Disability Index (SPADI), and overall patient satisfaction will be evaluated using the Global Perceived Effect (GPE) score. All parameters will be documented at baseline (before the procedure) and at follow-up visits on the 1st week, 4th week (1 month), and 3rd month post-procedure. The investigators aim to determine the efficacy, duration of effect, and safety profile of this intervention.",[60,28,61,62,63],"Chronic Shoulder Pain","Frozen Shoulder","Bursitis","Rotator Cuff Disorders",[65,66],"shoulder pain","pericapsular nerve group block","2026-05-21",{"date":69,"type":40},"2026-05-26",{"date":71,"type":21},"2026-06-01",{"date":73,"type":21},"2026-10-15",{"name":75,"class":47},"Ankara City Hospital Bilkent",1,{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":16,"minAge":84,"maxAge":18,"enrollmentInfo":85,"targetDuration":4,"studyType":22,"phases":87,"briefSummary":88,"conditions":89,"keywords":92,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":4},"100583641","comparison-of-peng-block-and-sificb-in-hip-fracture-surgeries-100583641","NCT06878963","COmparison of PENG Block and SIFICB in Hip Fracture Surgeries","Comparison of the Effects of Pericapsular Nerve Group Block and Suprainguinal Fascia Iliaca Compartment Block on Neuraxial Anesthesia Positioning and Postoperative Analgesia in Hip Fracture Surgeries","Inclusion Criteria:\n\n* Hip fractures\n* 40-80 years\n\nExclusion Criteria:\n\n* Contraindicated to spinal anesthesia\n* allergy to local anesthetics\n* severe peripheral neuropathy\n* mental disorders","40 Years",{"count":86,"type":21},150,[24],"The aim of this study is to compare the effectiveness of the PENG block and SIFIB in facilitating the positioning for neuroaxial anesthesia and their impact on the quality of postoperative analgesia.",[90,28,91],"Hip Fracture","Suprainguinal Fasya Iliaca Block",[93,94,95,96],"Hip fracture","Pericapsular nerve group block","Suprainguinal fasya iliaca block","Patient positioning","2025-03-11",{"date":99,"type":40},"2025-03-17",{"date":101,"type":21},"2025-04-01",{"date":103,"type":21},"2025-10-15",{"name":105,"class":47},"Adiyaman University Research Hospital"]