[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100624805":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":31,"locations":37,"responsibleParty":53,"collaborators":26,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":61,"acronym":26,"eligibilityCriteria":62,"healthyVolunteers":59,"sex":63,"minAge":64,"maxAge":65,"enrollmentInfo":66,"targetDuration":26,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":26,"overallStatus":76,"whyStopped":26,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"Stanford University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Choice","EXPERIMENTAL","Participants will select a preferred epidural regimen, receive routine epidural care, and complete brief in-hospital questionnaires about pain and overall satisfaction.",[13],"Procedure: Patient-selected epidural management",{"label":15,"type":16,"description":17,"interventionNames":18},"No-choice","ACTIVE_COMPARATOR","Participants will receive routine epidural care, and complete brief in-hospital questionnaires about pain and overall satisfaction.",[19],"Procedure: Standard epidural management",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"PROCEDURE","Patient-selected epidural management","Choice of epidural regimen",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Standard epidural management","Hospital's usual epidural regimen",[15],[32],{"name":33,"role":34,"phone":35,"phoneExt":26,"email":36},"Study Team","CONTACT","(650) 723-5403","brendan.carvalho@stanford.edu",[38],{"facility":39,"status":26,"city":40,"state":41,"zip":42,"country":43,"countryCode":44,"cosmosGeoPoint":45,"geoPoint":50,"contacts":51},"Lucile Packard Children's Hospital","Palo Alto","California","94304","United States","US",{"type":46,"coordinates":47},"Point",[48,49],-122.14302,37.44188,{"lat":49,"lon":48},[52],{"name":33,"role":34,"phone":35,"phoneExt":26,"email":36},{"type":54,"investigatorFullName":55,"investigatorTitle":56,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Brendan Carvalho","Professor of Anesthesiology, Perioperative and Pain Medicine","100624805","impact-of-patient-choice-for-epidural-potency-on-maternal-satisfaction-100624805",false,"NCT07414407","Impact of Patient Choice for Epidural Potency on Maternal Satisfaction","Inclusion Criteria:\n\n* Planned vaginal delivery\n* Patient requesting epidural labor analgesia\n* Gestational age \\>34 weeks\n\nExclusion Criteria:\n\n* Any contraindication to neuraxial block\n* History of chronic pain, anxiety or depression\n* Intolerance or allergy to local anesthetic or opioids\n* Cesarean delivery within 2 hours of epidural initiation","FEMALE","18 Years","50 Years",{"count":67,"type":68},150,"ESTIMATED","INTERVENTIONAL",[71],"NA","This clinical trial will compare two different approaches to epidural analgesia during labor to see which approach leads to higher patient satisfaction after delivery.\n\nPrimary aim: determine whether one approach produces greater postpartum maternal satisfaction.\n\nSecondary aims: compare pain control and side effects.\n\nParticipants are people in labor who receive epidural analgesia. They will receive routine clinical epidural care and complete brief, in-hospital questionnaires about pain and satisfaction.\n\nAll care is provided by the clinical team and safety practices remain unchanged.",[74,75],"Epidural Analgesia, Obstetric","Maternal Satisfaction","NOT_YET_RECRUITING","2026-02-10",{"date":79,"type":80},"2026-02-17","ACTUAL",{"date":82,"type":68},"2026-04-01",{"date":84,"type":68},"2030-12-31",{"name":5,"class":6},1]