[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100635010":3},{"organization":4,"outcomesModule":7,"designInfo":14,"detailedDescription":13,"studyPopulation":17,"armGroups":18,"interventions":27,"overallOfficials":13,"centralContacts":32,"locations":38,"responsibleParty":51,"collaborators":13,"id":54,"slug":13,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":13,"eligibilityCriteria":59,"healthyVolunteers":55,"sex":60,"minAge":61,"maxAge":62,"enrollmentInfo":63,"targetDuration":13,"studyType":66,"phases":13,"briefSummary":67,"conditions":68,"keywords":13,"overallStatus":70,"whyStopped":13,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"Istinye University","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":13},[9],{"measure":10,"description":11,"timeFrame":12},"Quality of Recovery-15 (QoR-15) Total Score","Quality of recovery will be assessed using the QoR-15 questionnaire. The total score ranges from 0 to 150, with higher scores indicating better recovery. The outcome will be compared between patients who received cervical plexus block and those who did not.","24 hours postoperatively",null,{"allocation":13,"interventionModel":13,"interventionModelDescription":13,"primaryPurpose":13,"observationalModel":15,"timePerspective":16,"maskingInfo":13},"CASE_CONTROL","PROSPECTIVE","Adults aged 18-75 years with ASA physical status I-III scheduled for elective bilateral total thyroidectomy under general anesthesia. Participants must be cognitively able to read Turkish and complete the QoR-15 questionnaire and provide written informed consent. Patients with chronic opioid use, chronic pain syndromes, psychiatric or neurological disorders, previous cervical surgery, planned extensive surgery, emergency procedures, pregnancy, or expected postoperative ICU need are excluded.",[19,22],{"label":20,"type":13,"description":21,"interventionNames":13},"Cervical Plexus Block Group","Patients who receive bilateral intermediate cervical plexus block as part of routine clinical practice, based on the attending anesthesiologist's decision.",{"label":23,"type":13,"description":24,"interventionNames":25},"No Block Group","Patients who do not receive cervical plexus block and are managed with standard postoperative analgesia according to routine clinical practice.",[26],"Other: Cervical Plexus Block",[28],{"type":6,"name":29,"description":30,"armGroupLabels":31,"otherNames":13},"Cervical Plexus Block","Bilateral intermediate cervical plexus block may be performed as part of routine clinical practice based on the attending anesthesiologist's decision. The study is observational, and no intervention, assignment, or protocol-driven procedure is applied. Patients are managed according to standard perioperative care.",[23],[33],{"name":34,"role":35,"phone":36,"phoneExt":13,"email":37},"İlke Dolgun","CONTACT","05555485632","ilkeser2004@gmail.com",[39],{"facility":40,"status":13,"city":41,"state":42,"zip":43,"country":44,"countryCode":13,"cosmosGeoPoint":45,"geoPoint":50,"contacts":13},"Istinye Üniversity","Istanbul","Merkez Mahallesi","34250","Turkey (Türkiye)",{"type":46,"coordinates":47},"Point",[48,49],28.94966,41.01384,{"lat":49,"lon":48},{"type":52,"investigatorFullName":34,"investigatorTitle":53,"investigatorAffiliation":5,"oldNameTitle":13,"oldOrganization":13},"PRINCIPAL_INVESTIGATOR","Assoc.Prof","100635010",false,"NCT07547124","Postoperative Analgesia and Recovery Quality in Total Thyroidectomy","Association Between Postoperative Analgesic Approaches and Quality of Recovery and Swallowing Pain in Patients Undergoing Elective Total Thyroidectomy: A Prospective Observational Study","Inclusion Criteria:\n\n* Patients aged 18-75 years\n* ASA physical status classification I-III\n* Patients scheduled for elective bilateral total thyroidectomy\n* Patients undergoing surgery under general anesthesia\n* Individuals able to read and understand Turkish and cognitively capable of completing the QoR-15 questionnaire\n* Patients providing written informed consent to participate in the study\n\nExclusion Criteria:\n\n* Chronic opioid use (≥3 months of regular opioid use)\n* Presence of chronic pain syndrome\n* Psychiatric illness or cognitive impairment\n* History of neurological disease (stroke, dementia, Parkinson's disease, etc.)\n* Known allergy to local anesthetic agents\n* Previous surgical interventions in the cervical region (including revision thyroid surgery)\n* Planned extended surgery with concomitant neck dissection\n* Substernal\u002Fretrosternal goiter cases (with potential need for sternotomy or additional procedures)\n* Emergency surgical procedures\n* Patients with ASA physical status IV or higher\n* Pregnancy\n* Patients expected to require postoperative intensive care\n* Patients experiencing intraoperative complications that deviate from the standard monitoring protocol","ALL","18 Years","65 Years",{"count":64,"type":65},100,"ESTIMATED","OBSERVATIONAL","This prospective observational study evaluates the association between postoperative analgesic approaches and recovery outcomes in patients undergoing elective total thyroidectomy. Patients will be followed under routine clinical care without intervention or randomization.\n\nThe primary outcome is the Quality of Recovery-15 (QoR-15) score at 24 hours. Secondary outcomes include swallowing pain, resting pain, opioid consumption, postoperative nausea and vomiting, and additional analgesic requirement.",[69],"Postoperative Pain","NOT_YET_RECRUITING","2026-04-20",{"date":73,"type":74},"2026-04-23","ACTUAL",{"date":76,"type":65},"2026-04-10",{"date":78,"type":65},"2026-09-10",{"name":5,"class":6},1]