Head-Only Draping in Pediatric Tonsillectomy

Part of paid clinical trials in New York, New York.

Sponsor
NYU Langone Health
Study ID
NCT07347301
Status
Not Yet Recruiting

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Conditions

  • Infections
  • Tonsillectomy

Eligibility Criteria

Sex
ALL
Age
N/A - 18 Years
Healthy Volunteers
Not accepted

Interventions

  • Full-Body Surgical Draping — OTHER
    Standard full-body drape.
  • Head-Only Surgical Draping — OTHER
    Use of head drape instead of full-body drape.

Study Details

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).

Key Dates

Start date
Feb 2, 2026
Status verified
Jan 2026
Primary completion
Aug 31, 2026
Completion
Dec 1, 2026

Study Design

Enrollment
200 participants (estimated)
Allocation
NA
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: Head-Only Draping
    Pediatric tonsillectomy will be performed with head-only draping.
  • Active Comparator: Full-Body Draping
    Pediatric tonsillectomy will be performed with traditional full-body draping.

Primary Outcome Measure

30-day postoperative infection rate [ Time Frame: Day 30 Post Operation ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
NYU Langone HealthNew YorkNew York10016-

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