← Eichor
Study identifier: NCT06670521 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Corticosteroids for Post-Extubation Dysphagia

Condition: Dysphagia · Laryngeal Edema  ·  Sponsor: University of Colorado, Denver

PhasePhase 2
Planned participants80
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a placebo-controlled, double-blind randomized trial of a short course of intravenous corticosteroids for Acute Respiratory Failure Survivors with Fiberoptic Endoscopic Evaluation of Swallowing (FEES) documented laryngeal edema. Study was leveraged using the existing R01 grant infrastructure COMIRB # 21-3873, study design, and research methods. Patients for the study proposed will have already been enrolled in the R01 longitudinal cohort study. The sites to perform this study include Colorado, BU, Yale, Tufts, and Stanford. Those R01-enrolled patients with laryngeal edema on their initial FEES examination: defined as the revised Patterson edema score greater than zero, will be approached for enrollment.

This description comes directly from the study's public registry record.

Talk to the study team

Anna Matheson, BSN  ·  4848836222  ·  anna.matheson@cuanschutz.edu

Jeffrey McKeehan, MSN  ·  3037246080  ·  jeffrey.mckeehan@cuanschutz.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of ColoradoAurora, Colorado, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06670521