[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100572569":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":35,"locations":41,"responsibleParty":59,"collaborators":26,"id":61,"slug":26,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":26,"eligibilityCriteria":66,"healthyVolunteers":62,"sex":67,"minAge":68,"maxAge":26,"enrollmentInfo":69,"targetDuration":26,"studyType":72,"phases":73,"briefSummary":75,"conditions":76,"keywords":26,"overallStatus":44,"whyStopped":26,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":89},{"fullName":5,"class":6},"Rutgers, The State University of New Jersey","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Superior laryngeal nerve block","EXPERIMENTAL","Patients will receive a superior laryngeal nerve block consisting of 1 milliliter of 0.25% bupivacaine and milliliter of triamcinolone acetate 40 mg\u002Fml to the neck on the side of the vocal cord lesion during their surgery.",[13],"Drug: Superior laryngeal nerve block - Intervention (Bupivacaine and triamcinolone acetonide suspension)",{"label":15,"type":16,"description":17,"interventionNames":18},"Placebo","PLACEBO_COMPARATOR","Patients will receive a placebo of 2 milliliter saline injection to the neck on the side of the vocal cord lesion during their surgery.",[19],"Drug: Superior laryngeal nerve block - Placebo (saline)",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DRUG","Superior laryngeal nerve block - Intervention (Bupivacaine and triamcinolone acetonide suspension)","Patients will receive a superior laryngeal nerve block consisting of 1 ml of 0.25% bupivacaine and 1mL of triamcinolone acetate 40 mg\u002Fml to the neck on the side of the vocal cord lesion during their surgery.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Superior laryngeal nerve block - Placebo (saline)","Patients will receive a saline placebo of 2mL saline to the neck on the side of the vocal cord lesion during their surgery.",[15],[32],{"name":33,"affiliation":5,"role":34},"Kenneth Yan, MD, PhD","PRINCIPAL_INVESTIGATOR",[36],{"name":37,"role":38,"phone":39,"phoneExt":26,"email":40},"Emma Thompson, MD","CONTACT","973-972-2548","ert46@njms.rutgers.edu",[42],{"facility":43,"status":44,"city":45,"state":46,"zip":47,"country":48,"cosmosGeoPoint":49,"geoPoint":54,"contacts":55},"Rutgers New Jersey Medical School","RECRUITING","Newark","New Jersey","07103","United States",{"type":50,"coordinates":51},"Point",[52,53],-74.17237,40.73566,{"lat":53,"lon":52},[56],{"name":57,"role":38,"phone":39,"phoneExt":26,"email":58},"Sandra Oxley","so514@njms.rutgers.edu",{"type":34,"investigatorFullName":33,"investigatorTitle":60,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"Assistant Professor, Laryngology","100572569",false,"NCT06734975","Effect of Superior Laryngeal Nerve Blocks on Patient Outcomes in Laryngeal Surgery","Effect of Intraoperative Superior Laryngeal Nerve Blocks on Patient Outcomes in Microdirect Laryngoscopy for Benign Vocal Fold Lesions: A Randomized Trial","Inclusion Criteria:\n\n* Patient is aged 18 years or older at time of consent\n* Patient has suspected or confirmed benign vocal fold lesion\n* Patient is planning to undergo direct laryngoscopy with excision of the vocal fold lesion\n* Patient is English or Spanish speaking\n* Patient is not pregnant per self report\n* Patient is not incarcerated\n\nExclusion Criteria:\n\n* Patient is not 18 years of age or older at consent date\n* Patient does not speak English or Spanish\n* Patient is currently pregnant or plans to become pregnant prior to their study procedure\n* Patient has a laryngeal malignancy or found to find a laryngeal malignancy on final pathology\n* Patient will not be undergoing direct laryngoscopy with excision of lesion\n* Patient is unable to provide consent or complete study activities\n* Patient is incarcerated","ALL","18 Years",{"count":70,"type":71},28,"ESTIMATED","INTERVENTIONAL",[74],"PHASE2","Patients undergoing surgery on their vocal cord will either receive a numbing injection to their throat or a saline injection during surgery. Symptoms such as how much coughing or pain patients have after surgery, as well as whether patient's voice gets better will be interrogated.",[77,78,79],"Vocal Cord Disease","Vocal Cord Polyp","Vocal Cord Cyst","2026-01-13",{"date":82,"type":83},"2026-01-15","ACTUAL",{"date":85,"type":83},"2025-07-11",{"date":87,"type":71},"2026-12",{"name":5,"class":6},1]