[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100637800":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":36,"locations":41,"responsibleParty":54,"collaborators":26,"id":58,"slug":59,"hasResults":60,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":64,"eligibilityCriteria":65,"healthyVolunteers":60,"sex":66,"minAge":67,"maxAge":68,"enrollmentInfo":69,"targetDuration":26,"studyType":72,"phases":73,"briefSummary":75,"conditions":76,"keywords":80,"overallStatus":43,"whyStopped":26,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":99},{"fullName":5,"class":6},"Saglik Bilimleri Universitesi","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Multimodal Fascial Plane Block Group","EXPERIMENTAL","Participants will receive a multimodal fascial plane block package consisting of bilateral superficial parasternal block, bilateral serratus anterior plane block, and adductor canal block following induction of general anesthesia and before surgical incision, in addition to standard perioperative analgesia.",[13],"Procedure: Multimodal Fascial Plane Block Package",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard Analgesia Group","ACTIVE_COMPARATOR","Participants will receive standard perioperative and postoperative analgesia without regional fascial plane block intervention.",[19],"Other: Standard Postoperative Analgesia",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"PROCEDURE","Multimodal Fascial Plane Block Package","Participants will receive ultrasound-guided bilateral superficial parasternal block, bilateral serratus anterior plane block, and adductor canal block after induction of general anesthesia and before surgical incision.",[9],null,{"type":6,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Standard Postoperative Analgesia","Participants will receive standard institutional perioperative and postoperative analgesia without regional fascial plane block.",[15],[32],{"name":33,"affiliation":34,"role":35},"Selen Topalel, MD","University of Health Sciences, Diyarbakir Gazi Yasargil Training and Research Hospital","PRINCIPAL_INVESTIGATOR",[37],{"name":33,"role":38,"phone":39,"phoneExt":26,"email":40},"CONTACT","+90 533 506 33 20","selentopalel26@gmail.com",[42],{"facility":34,"status":43,"city":44,"state":44,"zip":26,"country":45,"countryCode":26,"cosmosGeoPoint":46,"geoPoint":51,"contacts":52},"RECRUITING","Diyarbakır","Turkey (Türkiye)",{"type":47,"coordinates":48},"Point",[49,50],40.21721,37.91363,{"lat":50,"lon":49},[53],{"name":33,"role":38,"phone":39,"phoneExt":26,"email":40},{"type":35,"investigatorFullName":55,"investigatorTitle":56,"investigatorAffiliation":57,"oldNameTitle":26,"oldOrganization":26},"Selen Topalel","Anesthesiologist","Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital","100637800","multimodal-fascial-plane-block-for-postoperative-analgesia-in-isolated-cabg-surgery-100637800",false,"NCT07587320","Multimodal Fascial Plane Block for Postoperative Analgesia in Isolated CABG Surgery","Effect of Induction-Time Multimodal Fascial Plane Block on Postoperative Analgesia and Opioid Consumption in Patients Undergoing Isolated Coronary Artery Bypass Grafting: A Prospective Randomized Controlled Trial","BLOCKCABG","Inclusion Criteria:\n\n* Age between 18 and 80 years\n* Scheduled for elective isolated coronary artery bypass grafting (CABG) with saphenous vein graft harvesting\n* ASA physical status II-IV\n* Ability to provide written informed consent\n\nExclusion Criteria:\n\n* Known coagulopathy or contraindication to regional anesthesia\n* Use of anticoagulant therapy precluding regional block\n* Known allergy to local anesthetics\n* Local infection at planned block sites\n* Chronic opioid use or chronic pain syndrome\n* Emergency surgery\n* Redo sternotomy\n* Severe neurological disorder affecting pain assessment","ALL","18 Years","80 Years",{"count":70,"type":71},56,"ESTIMATED","INTERVENTIONAL",[74],"NA","Postoperative pain following coronary artery bypass grafting (CABG) via median sternotomy remains a significant clinical problem and is associated with increased opioid consumption and postoperative complications. Fascial plane blocks have emerged as part of multimodal analgesia strategies in cardiac surgery.\n\nThis prospective, randomized, controlled, single-blinded study aims to evaluate the effect of an induction-time multimodal fascial plane block package-consisting of bilateral superficial parasternal block, bilateral serratus anterior plane block, and adductor canal block-on postoperative analgesia, opioid consumption, and clinical outcomes in patients undergoing elective isolated CABG with saphenous vein graft harvesting.\n\nPatients will be randomized in a 1:1 ratio to receive either the multimodal fascial plane block package in addition to standard postoperative analgesia or standard postoperative analgesia alone. The primary outcome is total opioid consumption within the first 24 postoperative hours. Secondary outcomes include pain scores, time to first opioid requirement, extubation time, postoperative pulmonary complications, atrial fibrillation, and length of ICU and hospital stay.",[77,78,79],"Coronary Artery Bypass Graft (CABG)","Postoperative Pain","Sternotomy",[81,82,83,84,85,86,87,88,89],"Parasternal Block","Serratus Anterior Plane Block","Adductor Canal Block","Opioid Consumption","Multimodal Analgesia","Randomized Controlled Trial","Cardiac Surgery","Fascial Plane Block","Coronary Artery Bypass Graft","2026-05-12",{"date":92,"type":93},"2026-05-14","ACTUAL",{"date":95,"type":93},"2026-01-01",{"date":97,"type":71},"2026-09",{"name":5,"class":6},1]