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Respiratory-Swallow Coordination in Cardiothoracic Surgical Patients

A Preliminary Investigation of Respiratory-Swallow Coordination in Cardiothoracic Surgical Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05173207
Enrollment
8
Registered
2021-12-29
Start date
2022-03-03
Completion date
2022-07-27
Last updated
2022-07-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases, Thoracic Diseases

Keywords

Dysphagia, Extubation, Respiratory-swallow coordination, Swallow

Brief summary

Dysphagia (swallowing impairment) is a common complication of cardiothoracic surgery (CS). Although alterations in respiratory-swallow coordination is a known underlying pathophysiologic mechanism of dysphagia in multiple patient populations, no group has examined respiratory-swallow physiology in CS patients. The proposed study will examine respiratory-swallow physiology in CS patients and determine its association with unsafe swallowing and inferior health-related outcomes.

Detailed description

The proposed study will examine respiratory-swallow physiology in cardiothoracic surgical patients and determine its association with unsafe swallowing and inferior health-related outcomes. Participation will involve a single postoperative research exam of approximately 60-90 minute duration. Participants will be seated upright and positioned for simultaneous instrumental imaging of swallow physiology, nasal airflow monitoring, and respiratory inductance plethysmography testing.

Interventions

DIAGNOSTIC_TESTVideofluoroscopic swallow exam with concurrent monitoring of respiratory-swallow coordination

Participants will undergo simultaneous videofluoroscopy, nasal airflow and respiratory inductance plethysmography testing.

Sponsors

University of Florida
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Adults over 18 years of age who have undergone cardiothoracic surgery at UF Health * No allergies to barium * Not pregnant * Willing to participate in study

Exclusion criteria

* Individuals 18 years of age or younger * Allergies to barium * Pregnant * Not willing to participate in study

Design outcomes

Primary

MeasureTime frameDescription
Penetration Aspiration ScaleUp to 1 yearThis scale is a validated measure used by trained blinded clinicians to assign ratings of safety to swallowing bolus trials. The development and use of an 8-point, equal-appearing interval scale (8 being best; 1 being worst) to describe penetration and aspiration events are described. Scores are determined primarily by the depth to which material passes in the airway and by whether or not material entering the airway is expelled.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026