[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100653773":3},{"organization":4,"outcomesModule":7,"designInfo":41,"detailedDescription":40,"studyPopulation":44,"armGroups":45,"interventions":59,"overallOfficials":40,"centralContacts":65,"locations":71,"responsibleParty":86,"collaborators":90,"id":94,"slug":95,"hasResults":96,"nctId":97,"briefTitle":98,"officialTitle":99,"acronym":100,"eligibilityCriteria":101,"healthyVolunteers":96,"sex":102,"minAge":103,"maxAge":40,"enrollmentInfo":104,"targetDuration":40,"studyType":107,"phases":40,"briefSummary":108,"conditions":109,"keywords":113,"overallStatus":73,"whyStopped":40,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":129},{"fullName":5,"class":6},"Bursa City Hospital","OTHER_GOV",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":40},[9],{"measure":10,"description":11,"timeFrame":12},"Obstetric Quality of Recovery-10 Score","Postoperative recovery quality will be assessed using the Turkish version of the Obstetric Quality of Recovery-10 questionnaire. Total scores range from 0 to 100, with higher scores indicating better recovery.","24 hours after cesarean delivery",[14,18,22,26,30,34,37],{"measure":15,"description":16,"timeFrame":17},"Enhanced Recovery Protocol Compliance","Overall compliance with enhanced recovery protocol components will be calculated as the percentage of completed preoperative, intraoperative, and postoperative components.","From the preoperative assessment to 24 hours after cesarean delivery",{"measure":19,"description":20,"timeFrame":21},"Postoperative Pain Intensity","Pain intensity will be assessed using the Numeric Rating Scale, ranging from 0 to 10, with higher scores indicating greater pain intensity.","In the recovery unit and at 2, 6, 12, and 24 hours after cesarean delivery",{"measure":23,"description":24,"timeFrame":25},"Rescue Opioid Requirement","The number of participants requiring rescue opioid medication after cesarean delivery will be recorded.","During the first 24 hours after cesarean delivery",{"measure":27,"description":28,"timeFrame":29},"Total Amsterdam Preoperative Anxiety and Information Scale Score","The overall Amsterdam Preoperative Anxiety and Information Scale score will be calculated. Scores range from 6 to 30, with higher scores indicating greater anxiety and information needs.","Before cesarean delivery",{"measure":31,"description":32,"timeFrame":33},"Length of Hospital Stay","Duration of hospital stay from the completion of cesarean delivery until formal hospital discharge, measured in hours.","From cesarean delivery until hospital discharge, assessed up to 7 days",{"measure":35,"description":36,"timeFrame":29},"Preoperative Information Requirement","Preoperative information needs will be evaluated using the information subscale of the Amsterdam Preoperative Anxiety and Information Scale. Scores range from 2 to 10, with higher scores indicating greater information needs.",{"measure":38,"description":39,"timeFrame":29},"Preoperative Anxiety","Preoperative anxiety will be evaluated using the anxiety subscale of the Amsterdam Preoperative Anxiety and Information Scale. Scores range from 4 to 20, with higher scores indicating greater anxiety.",null,{"allocation":40,"interventionModel":40,"interventionModelDescription":40,"primaryPurpose":40,"observationalModel":42,"timePerspective":43,"maskingInfo":40},"COHORT","PROSPECTIVE","Adult pregnant women aged 18 years or older undergoing elective cesarean delivery under spinal anesthesia at Bursa City Hospital, Türkiye. Eligible participants will have American Society of Anesthesiologists physical status II or III and will be enrolled consecutively during the study period.",[46,51,55],{"label":47,"type":40,"description":48,"interventionNames":49},"High ERAC Compliance","Women undergoing elective cesarean delivery under spinal anesthesia with adherence to 80% or more of enhanced recovery protocol components.",[50],"Other: Assessment of Enhanced Recovery Protocol Compliance",{"label":52,"type":40,"description":53,"interventionNames":54},"Moderate ERAC Compliance","Women undergoing elective cesarean delivery under spinal anesthesia with adherence to 60% to 79% of enhanced recovery protocol components.",[50],{"label":56,"type":40,"description":57,"interventionNames":58},"Low ERAC Compliance","Women undergoing elective cesarean delivery under spinal anesthesia with adherence to less than 60% of enhanced recovery protocol components.",[50],[60],{"type":61,"name":62,"description":63,"armGroupLabels":64,"otherNames":40},"OTHER","Assessment of Enhanced Recovery Protocol Compliance","Adherence to routinely implemented enhanced recovery after cesarean delivery components will be assessed during the preoperative, intraoperative, and postoperative periods. Each completed component will receive one point, and overall adherence will be calculated as a percentage. No additional interventions will be administered.",[47,56,52],[66],{"name":67,"role":68,"phone":69,"phoneExt":40,"email":70},"emre ulusoy, MD","CONTACT","05379492799","emreulusoy36@gmail.com",[72],{"facility":5,"status":73,"city":74,"state":75,"zip":76,"country":77,"countryCode":40,"cosmosGeoPoint":78,"geoPoint":83,"contacts":84},"RECRUITING","Bursa","Nilüfer","16110","Turkey (Türkiye)",{"type":79,"coordinates":80},"Point",[81,82],29.06013,40.19559,{"lat":82,"lon":81},[85],{"name":67,"role":68,"phone":69,"phoneExt":40,"email":70},{"type":87,"investigatorFullName":88,"investigatorTitle":89,"investigatorAffiliation":5,"oldNameTitle":40,"oldOrganization":40},"PRINCIPAL_INVESTIGATOR","eralp çevikkalp","Associate Professor of Anesthesiology and Reanimation, M.D.",[91],{"name":92,"class":93},"Ulusoy, Emre, M.D.","INDIV","100653773","enhanced-recovery-protocol-compliance-and-quality-of-recovery-after-cesarean-delivery-100653773",false,"NCT07790471","Enhanced Recovery Protocol Compliance and Quality of Recovery After Cesarean Delivery","Effect of Enhanced Recovery After Cesarean Delivery Protocol Compliance on Postoperative Quality of Recovery in Patients Undergoing Cesarean Delivery Under Spinal Anesthesia: A Prospective Observational Study","ERAC-QoR","Inclusion Criteria:\n\n* Age 18 years or older\n* Scheduled for elective cesarean delivery\n* Planned spinal anesthesia\n* American Society of Anesthesiologists physical status II or III\n* Ability to read and understand Turkish\n* Provision of written informed consent\n\nExclusion Criteria:\n\n* Emergency cesarean delivery\n* General anesthesia or conversion from spinal to general anesthesia\n* Major obstetric hemorrhage\n* Requirement for postoperative intensive care\n* Chronic opioid use\n* Chronic pain syndrome\n* Severe psychiatric disease\n* Severe neurological disease\n* Inability to communicate\n* Cognitive impairment preventing completion of study questionnaires\n* Refusal to participate","FEMALE","18 Years",{"count":105,"type":106},150,"ESTIMATED","OBSERVATIONAL","This prospective observational study will evaluate whether adherence to enhanced recovery after cesarean delivery protocols is associated with postoperative recovery quality in women undergoing elective cesarean delivery under spinal anesthesia. A total of 150 participants will be enrolled. Recovery quality will be assessed using the Turkish version of the Obstetric Quality of Recovery-10 questionnaire at 24 hours after surgery. Pain, opioid use, nausea, mobilization, oral intake, breastfeeding, and patient satisfaction will also be evaluated.",[110,111,112],"Cesarean Section","Postoperative Recovery","Postoperative Pain",[114,115,116,117,118,119,38],"Enhanced Recovery After Cesarean Delivery","ERAC","Obstetric Quality of Recovery","ObsQoR-10","Spinal Anesthesia","Maternal Recovery","2026-08-25",{"date":122,"type":123},"2026-08-27","ACTUAL",{"date":125,"type":123},"2026-08-15",{"date":127,"type":106},"2026-10-15",{"name":5,"class":6},1]