NCT07635719
Coblator Wand Comparative Analysis
Recruiting
NAAges 1–18InterventionalMontefiore Medical CenterInvestigator-initiated
~30 participants
Updated 2026-07-31 on ClinicalTrials.gov
What's tested:New Coblator Ablation WandsReprocessed Medline Coblator Ablation Wands
At a glance
Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Surgeon Comfort
Measured over Following the procedure, up to 4 hours
Conditions
Where it's being run
1 sites across 1 statesNew York1
Study leadership
- John Bent, MD · PRINCIPAL_INVESTIGATOR · Montefiore Medical Center
Who to contact
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Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Pediatric patients scheduled for tonsillectomy and/or adenoidectomy
Parental consent and child assent (when applicable)
Exclusion
Pregnancy
What this trial measures
- Surgeon ComfortFollowing the procedure, up to 4 hours
The primary outcome for this study is surgeon comfort in terms of using the new or reprocessed coblator wand again based on data collected from the post-procedure surveys. Surgeon comfort will be assessed as a dichotomous (yes/no) measure following the procedure. The number of instances for which the surgeon is comfortable using the new or reprocessed coblator wand will be summarized by study arm using descriptive statistics.