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NCT04537650 · ClinicalTrials.gov registry record

Swallowing Impairment After COVID-19 Infection

A clinical trial, sponsored by University Health Network, Toronto.

Completed
Registry status
44
Enrollment target

NCT04537650: Completed study, sponsored by University Health Network, Toronto.

NCT04537650 is a clinical trial that has completed, run by University Health Network, Toronto. The registered enrollment target is 44 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04537650 has completed, sponsored by University Health Network, Toronto.

COMPLETED
Registry status
44 participants
Enrollment target

Study Summary

This is an observational study, in which people recovering from COVID-19 infection will attend an outpatient clinic for a comprehensive swallowing assessment. The assessment will include a videofluoroscopy, measurement of respiratory-swallow coordination using a digital stethoscope, measures of tongue and cough strength and patient reported measures that will help us to understand the presence and impact of swallowing impairment (dysphagia) in this population.

Primary Outcome

Frequency of participants demonstrating airway invasion on thin liquids, defined as Penetration-Aspiration Scale score of 3 and higher (Rosenbek et al., 1996). Higher scores indicate worse function.

Interventions

  • DIAGNOSTIC_TEST Videofluoroscopic Swallowing Study (VFSS)

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2021-01-01
Est. Completion 2022-03-31
University Health Network, Toronto

23 total trials

What the finished NCT04537650 record still lists

NCT04537650 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 44 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Videofluoroscopic Swallowing Study (VFSS) is the first listed.

NCT04537650 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04537650 about?

NCT04537650 is a clinical study titled "Swallowing Impairment After COVID-19 Infection". This is an observational study, in which people recovering from COVID-19 infection will attend an outpatient clinic for a comprehensive swallowing assessment. The assessment will include a videofluoroscopy, measurement of respiratory-swallow coordination using a digital stethoscope, measures of tong...

What is the current status of trial NCT04537650?

This trial is currently completed. The enrollment target is 44 participants. The study started on 2021-01-01. Estimated completion is 2022-03-31.

What interventions are being tested in trial NCT04537650?

The interventions under investigation include: Videofluoroscopic Swallowing Study (VFSS) (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT04537650?

This trial is sponsored by University Health Network, Toronto, which has 23 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT04537650, the US trial registry maintained by the National Library of Medicine. NCT04537650 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.