NCT07057258

Injection Versus Suture Repair of Laryngeal Clefts

Enrolling by Invitation
NAAges 12–10InterventionalTreatment
Oregon Health and Science University
~128 participants
Updated 2025-09-29 on ClinicalTrials.gov
What's tested:Endoscopic suture repairInjection laryngoplasty

At a glance

Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Resolution of penetration/aspiration
Measured over 3 months post operative
Laryngeal Cleft
Dysphagia
2 sites across 2 states
Oregon1
Tennessee1

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

children aged 12 months - 10 years referred to a multi-disciplinary aerodigestive clinic with evidence of penetration or aspiration on VFSS, requiring any amount of thickening of liquids and unable to wean after 2-month trial of thickened liquids.

Exclusion

Cerebral palsy
Down syndrome
Prematurity \< 28 weeks gestational age
Hypoxic brain injury
Any syndrome with significant hypotonia
History of nothing by mouth (NPO) for \> 1 month prior to assessment
\>50% of nutrition by G-tube
Tracheostomy
History of prior IL or ER
  • Resolution of penetration/aspiration3 months post operative

    No thickener needed on speech pathologist assessment of video fluoroscopic swallow study