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Dysphagia and VFMI in Cardiac Patients
NCT03768739 · View on ClinicalTrials.gov ↗
Study Summary
The proposed study seeks to determine the incidence of dysphagia and vocal fold mobility impairment (VFMI) in individuals undergoing cardiothoracic surgical procedures. It also seeks to determine the impact of postoperative swallowing impairment on health-related outcomes.
Conditions Studied
Interventions
- PROCEDURE Fiberoptic Endoscopic Evaluation of Swallowing
Study Locations (3)
Florida
- Cardiovascular Clinic at UF Health UF — Gainesville
- UF Health at the University of Florida — Gainesville
- Thoracic and Cardiovasscular Surgery at UF Health — Gainesville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 207 participants |
| Start Date | 2019-02-03 |
| Est. Completion | 2020-09-02 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03768739
The ClinicalTrials.gov registry entry for NCT03768739 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 207 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Florida, which has 1,066 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Cardiac Disease appearing as the primary indexed condition, and to 1 intervention — of which Fiberoptic Endoscopic Evaluation of Swallowing is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03768739 reports 3 study locations spanning 1 distinct geographic area — top geographies include Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03768739 about?
NCT03768739 is a clinical study titled "Dysphagia and VFMI in Cardiac Patients". The proposed study seeks to determine the incidence of dysphagia and vocal fold mobility impairment (VFMI) in individuals undergoing cardiothoracic surgical procedures. It also seeks to determine the impact of postoperative swallowing impairment on health-related outcomes.
What is the current status of trial NCT03768739?
This trial is currently completed. The enrollment target is 207 participants. The study started on 2019-02-03. Estimated completion is 2020-09-02.
What conditions does trial NCT03768739 study?
This clinical trial studies the following conditions: Cardiac Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03768739?
The interventions under investigation include: Fiberoptic Endoscopic Evaluation of Swallowing (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03768739?
This trial is sponsored by University of Florida, which has 1,066 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03768739 being conducted?
This trial has 3 study locations across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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