[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100635121":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":30,"centralContacts":38,"locations":44,"responsibleParty":60,"collaborators":30,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":70,"eligibilityCriteria":71,"healthyVolunteers":66,"sex":72,"minAge":73,"maxAge":30,"enrollmentInfo":74,"targetDuration":30,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":83,"overallStatus":47,"whyStopped":30,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":101},{"fullName":5,"class":6},"National and Kapodistrian University of Athens","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Short-axis femoral artery block","EXPERIMENTAL","Ultrasound-guided femoral artery block using short-axis in-plane technique with 10 mL ropivacaine 0.5%.",[13],"Procedure: Femoral artery block - short-axis",{"label":15,"type":10,"description":16,"interventionNames":17},"Long-axis femoral artery block","Ultrasound-guided femoral artery block using long-axis in-plane technique with 10 mL ropivacaine 0.5%.",[18],"Procedure: Femoral artery block - long-axis",{"label":20,"type":21,"description":22,"interventionNames":23},"Saline control injection","PLACEBO_COMPARATOR","Ultrasound-guided femoral artery injection using in-plane technique with 10 mL 0.9% normal saline.",[24],"Other: Normal saline injection (control)",[26,31,34],{"type":27,"name":28,"description":11,"armGroupLabels":29,"otherNames":30},"PROCEDURE","Femoral artery block - short-axis",[9],null,{"type":27,"name":32,"description":16,"armGroupLabels":33,"otherNames":30},"Femoral artery block - long-axis",[15],{"type":6,"name":35,"description":36,"armGroupLabels":37,"otherNames":30},"Normal saline injection (control)","Ultrasound-guided femoral artery injection using 10 mL 0.9% normal saline.",[20],[39],{"name":40,"role":41,"phone":42,"phoneExt":30,"email":43},"LAMPRINI BANASIOU","CONTACT","+306981809083","banasiou_labrini@yahoo.com",[45],{"facility":46,"status":47,"city":48,"state":30,"zip":49,"country":50,"countryCode":51,"cosmosGeoPoint":52,"geoPoint":57,"contacts":58},"University General Hospital Attikon","RECRUITING","Athens","124 61","Greece","GR",{"type":53,"coordinates":54},"Point",[55,56],23.72784,37.98376,{"lat":56,"lon":55},[59],{"name":40,"role":41,"phone":42,"phoneExt":30,"email":43},{"type":61,"investigatorFullName":62,"investigatorTitle":63,"investigatorAffiliation":5,"oldNameTitle":30,"oldOrganization":30},"PRINCIPAL_INVESTIGATOR","Banasiou Lamprini","Principal Investigator","100635121","a-long-axis-approach-to-the-femoral-artery-block-fab-for-managing-tourniquet-pain-and-hypertension-in-below-the-knee-fracture-surgery-100635121",false,"NCT07548567","A Long Axis Approach to the Femoral Artery Block (FAB) for Managing Tourniquet Pain and Hypertension in Below-the-Knee Fracture Surgery","Turning the Probe, Changing the View: A Novel Long Axis Approach to the Femoral Artery Block (FAB) for Managing Tourniquet Pain and Hypertension in Below-the-Knee Fracture Surgery: A Prospective, Randomized, Double-Blind Controlled Trial","FAB","Inclusion Criteria:\n\n* Age \\>18 years\n* Physical status ASA I-III\n* Fluent in Greek or English\n* Scheduled surgery: below-knee fractures\n* Tourniquet duration ≥45 minutes\n\nExclusion Criteria:\n\n* Refusal to participate\n* Local inflammation at block site\n* Known allergy to study drugs\n* Morbid obesity (BMI \\>40)\n* Communication inability\n* Systemic neurological disease affecting peripheral nerves\n* Chronic pain therapy\n* Diabetic neuropathy\n* Uncontrolled hypertension","ALL","18 Years",{"count":75,"type":76},84,"ESTIMATED","INTERVENTIONAL",[79],"NA","This is a prospective, randomized, double-blind controlled trial evaluating an ultrasound-guided femoral artery block (FAB) using a long-axis in-plane approach compared with a short-axis approach and a control group.\n\nThe study will include adult patients (ASA I-III) undergoing below-the-knee fracture surgery with tourniquet application. All patients will receive standardized anesthesia including sciatic nerve block and total intravenous anesthesia.\n\nParticipants will be randomized into three groups: short-axis FAB, long-axis FAB, or control (saline injection). The primary aim is to assess the effectiveness of the long-axis FAB in reducing tourniquet-induced hypertension. Secondary outcomes include hemodynamic stability, analgesic requirements, pain scores, block characteristics, and procedural performance metrics.",[82],"Tourniquet Hypertension",[84,85,86,87,88,89,90,91],"FAB block","Tourniquet-induced hypertension","Tourniquet pain","Below-knee fracture surgery","Sympathetic blockade","intraoperative hypertension","sciatic nerve block","randomized controlled trial","2026-07-02",{"date":94,"type":95},"2026-07-06","ACTUAL",{"date":97,"type":95},"2026-06-03",{"date":99,"type":76},"2028-02",{"name":5,"class":6},1]