[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100646279":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":10,"centralContacts":15,"locations":10,"responsibleParty":24,"collaborators":10,"id":26,"slug":27,"hasResults":28,"nctId":29,"briefTitle":30,"officialTitle":31,"acronym":10,"eligibilityCriteria":32,"healthyVolunteers":28,"sex":33,"minAge":34,"maxAge":35,"enrollmentInfo":36,"targetDuration":10,"studyType":39,"phases":10,"briefSummary":40,"conditions":41,"keywords":10,"overallStatus":44,"whyStopped":10,"lastUpdateSubmitDate":45,"lastUpdatePostDateStruct":46,"startDateStruct":49,"completionDateStruct":51,"leadSponsor":53,"locationsCount":10},{"fullName":5,"class":6},"Samsun University","OTHER",[8,12],{"label":9,"type":10,"description":11,"interventionNames":10},"Group-SPSİPB",null,"The Serratus Posterior Superior Intercostal Plane Block (SPSIPB) will be administered under ultrasound guidance 30 minutes before the induction of anesthesia for anterior cervical discectomy and fusion (ACDF) surgery.",{"label":13,"type":10,"description":14,"interventionNames":10},"Group-Control","Patients in the control group will not receive any regional anesthesia technique before surgery and will undergo anterior cervical discectomy and fusion (ACDF) surgery under standard general anesthesia. Postoperative pain management will be provided according to the institution's routine multimodal analgesia protocol.",[16,21],{"name":17,"role":18,"phone":19,"phoneExt":10,"email":20},"HALE KEFELİ ÇELİK","CONTACT","5057242409","ck_hale@hotmail.com",{"name":22,"role":18,"phone":10,"phoneExt":10,"email":23},"Betül Çiftçi Kurt","betulciftcikurt@gmail.com",{"type":25,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100646279","postoperative-outcomes-of-regional-blocks-in-cervical-disc-surgery-100646279",false,"NCT07694180","Postoperative Outcomes of Regional Blocks in Cervical Disc Surgery","Postoperative Outcomes of Regional Blocks Performed in Cervical Disc Surgery: A Prospective Observational Study","Inclusion Criteria:\n\n* Patients aged between 18 and 70 years.\n* American Society of Anesthesiologists (ASA) physical status I, II, or III.\n* Patients scheduled for elective anterior cervical discectomy and fusion (ACDF) surgery under general anesthesia.\n* Patients who provide written informed consent and agree to participate in the study.\n\nExclusion Criteria:\n\n* Patients with a history of bleeding diathesis or those receiving anticoagulant therapy.\n* Patients with a known allergy or hypersensitivity to local anesthetics or opioid medications.\n* Patients with infection at the planned block site.\n* Patients with a history of previous cervical spine surgery.\n* Patients with a history of gabapentinoid or corticosteroid use within the last 3 weeks.","ALL","18 Years","70 Years",{"count":37,"type":38},66,"ESTIMATED","OBSERVATIONAL","The aim of this study is to evaluate the postoperative analgesic efficacy of the Serratus Posterior Superior Intercostal Plane Block (SPSIP block) in patients undergoing Anterior Cervical Discectomy and Fusion (ACDF) surgery and to compare the outcomes with those of patients who do not receive regional anesthesia.",[42,43],"Acute Pain","Servical Disc Herniation","NOT_YET_RECRUITING","2026-07-02",{"date":47,"type":48},"2026-07-09","ACTUAL",{"date":50,"type":38},"2026-06-22",{"date":52,"type":38},"2027-01-02",{"name":5,"class":6}]