[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100613555":3},{"organization":4,"armGroups":7,"interventions":17,"overallOfficials":11,"centralContacts":23,"locations":11,"responsibleParty":29,"collaborators":11,"id":33,"slug":34,"hasResults":35,"nctId":36,"briefTitle":37,"officialTitle":38,"acronym":11,"eligibilityCriteria":39,"healthyVolunteers":35,"sex":40,"minAge":41,"maxAge":11,"enrollmentInfo":42,"targetDuration":11,"studyType":45,"phases":46,"briefSummary":48,"conditions":49,"keywords":51,"overallStatus":54,"whyStopped":11,"lastUpdateSubmitDate":55,"lastUpdatePostDateStruct":56,"startDateStruct":59,"completionDateStruct":61,"leadSponsor":63,"locationsCount":11},{"fullName":5,"class":6},"Beth Israel Deaconess Medical Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Topical lidocaine","EXPERIMENTAL",null,[13],"Drug: topical vaginal application lidocaine gel",{"label":15,"type":16,"description":11,"interventionNames":11},"Standard of care","NO_INTERVENTION",[18],{"type":19,"name":20,"description":21,"armGroupLabels":22,"otherNames":11},"DRUG","topical vaginal application lidocaine gel","Application of topical vaginal lidocaine prior to cervical balloon ripening",[9],[24],{"name":25,"role":26,"phone":27,"phoneExt":11,"email":28},"Sarah Little, MD","CONTACT","6176677000","slittl10@bidmc.harvard.edu",{"type":30,"investigatorFullName":31,"investigatorTitle":32,"investigatorAffiliation":5,"oldNameTitle":11,"oldOrganization":11},"PRINCIPAL_INVESTIGATOR","Sarah Little","Associate Professor","100613555","phase-2-pain-control-for-cervical-ripening-balloon-100613555",false,"NCT07268118","Pain Control for Cervical Ripening Balloon","Randomized Control Trial for Pain Control With Topical Lidocaine for Cervical Ripening Balloon Placement","Inclusion Criteria:\n\n* Age ≥18 years\n* Gestational age ≥37 weeks\n* Viable pregnancy\n* Intact membranes\n* English speaking\n* Interested in cervical ripening balloon placement\n* Able to provide consent\n\nExclusion Criteria:\n\n* Allergy or sensitivity to lidocaine\n* Patients that already have neuraxial anesthesia (i.e. spinal, epidural, combined spinal\u002Fepidural)\n* Known uterine or cervical anomalies","FEMALE","18 Years",{"count":43,"type":44},110,"ESTIMATED","INTERVENTIONAL",[47],"PHASE2","No standard of care exists for pain management during cervical ripening balloon placement. The purpose of this study is to evaluate if vaginal topical lidocaine reduces pain related to cervical ripening balloon placement during induction of labor.",[50],"Labor Induction",[52,53],"cervical ripening","cervical balloon","NOT_YET_RECRUITING","2026-03-03",{"date":57,"type":58},"2026-03-05","ACTUAL",{"date":60,"type":44},"2026-04",{"date":62,"type":44},"2027-06",{"name":5,"class":6}]