[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT07347301":3,"trial-entities:NCT07347301":17,"trial-summary:NCT07347301":17},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":7,"overall_status":8,"completion_date":9,"status_verified_date":10,"last_update_date":11,"start_date":12,"sponsor_name":13,"lead_sponsor_class":14,"has_dmc":15,"brief_summary":16,"detailed_description":17,"conditions":18,"keywords":21,"study_type":22,"primary_purpose":23,"phases":24,"enrollment_info":26,"interventions":29,"primary_outcomes":40,"secondary_outcomes":44,"sex":50,"minimum_age":17,"maximum_age":51,"healthy_volunteers":15,"eligibility_criteria":52,"std_ages":56,"locations":59,"central_contacts":67,"overall_officials":73,"references":76,"see_also_links":77},"NCT07347301","25-01372","Head-Only Draping in Pediatric Tonsillectomy","30-Day Postoperative Infection Rate in Pediatric Tonsillectomy: Head-Drape vs. Full-Body Surgical Draping","NOT_YET_RECRUITING","2026-12-01","2026-01","2026-01-16","2026-02-02","NYU Langone Health","OTHER",false,"This single-center, interventional study will compare 30-day postoperative infection rates in pediatric tonsillectomy performed with either head-only draping or traditional full-body draping. Secondary analyses will evaluate differences in waste production, material and disposal costs, and provider attitudes between the two draping techniques. This study will randomize participants 1:1 to either the head-only draping cohort (intervention) or the full-body draping cohort (control).",null,[19,20],"Tonsillectomy","Infections",[],"INTERVENTIONAL","SUPPORTIVE_CARE",[25],"NA",{"count":27,"type":28},200,"ESTIMATED",[30,35],{"type":14,"name":31,"description":32,"armGroupLabels":33},"Full-Body Surgical Draping","Standard full-body drape.",[34],"Full-Body Draping",{"type":14,"name":36,"description":37,"armGroupLabels":38},"Head-Only Surgical Draping","Use of head drape instead of full-body drape.",[39],"Head-Only Draping",[41],{"measure":42,"timeFrame":43},"30-day postoperative infection rate","Day 30 Post Operation",[45,48],{"measure":46,"timeFrame":47},"Total weight of waste","Day 0 (Day of Operation)",{"measure":49,"timeFrame":47},"Disposal costs","ALL","18 Years",{"inclusion":53,"exclusion":54,"raw_text":55},[],[],"Inclusion Criteria:\n\n1. Pediatric patients \\\u003C18 years at time of surgery.\n2. Scheduled for tonsillectomy, with or without adenoidectomy, without any other procedures requiring full-body draping.\n3. Ability to complete 30-day outcome assessment (i.e., remain in follow-up or reachable via phone\u002Felectronic health record).\n4. Parent\u002Fguardian able to provide parental permission and consent for both them and their children.\n\nExclusion Criteria:\n\n1. Significant deviation from planned surgical technique during case.\n2. Pre-existing systemic infection prior to surgery.\n3. Known immunodeficiency or current systemic immunosuppressive therapy.",[57,58],"CHILD","ADULT",[60],{"facility":13,"city":61,"state":61,"zip":62,"country":63,"geoPoint":64},"New York","10016","United States",{"lat":65,"lon":66},40.71427,-74.00597,[68],{"name":69,"role":70,"phone":71,"email":72},"Neelima Tummala, MD","CONTACT","646-501-7890","neelima.tummala@nyulangone.org",[74],{"name":69,"affiliation":13,"role":75},"PRINCIPAL_INVESTIGATOR",[],[]]