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NCT05603897 · ClinicalTrials.gov registry record · NA
Non-standardized vs. Standardized Screening for Dysphagia
A NA study of Dysphagia, sponsored by University of Miami.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT05603897: Recruiting NA study of Dysphagia, sponsored by University of Miami.
NCT05603897 is a NA study of Dysphagia that is actively recruiting participants, run by University of Miami. The registered enrollment target is 50 participants, below the 171-participant average among 35 other Dysphagia trials with a reported enrollment target (71% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05603897, a NA study of Dysphagia, is actively recruiting participants, sponsored by University of Miami.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to compare two different screening tests for detecting dysphagia (difficulty swallowing) as well as the risk for aspiration (silent swallowing of liquids/solids into the lungs) in patients after an ischemic stroke (when a blood clot blocks or narrows an artery leading to the brain).
Primary Outcome
The MASA is a 24-item clinical test that evaluates swallowing in the order in which swallowing phases occur. Each item is quantitatively scored using either a 5-point or 10-point score at the end of which a total score out of 200 is summed up. The MASA takes approximately 15-20 minutes to perform and can then be repeated during a patient's clinical course to monitor for recovery.
Conditions Studied
Interventions
- OTHER Mann Assessment of Swallowing Ability (MASA) (dysphagia screening tool)
- OTHER Non-standardized clinical swallow evaluation
Study Locations (1)
Florida
- Lynn Rehabilitation Center / University of Miami - Miami
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2024-04-05 |
| Est. Completion | 2026-01-30 |
| Phase | NA |
What NCT05603897 shows while recruiting
NCT05603897 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 171-participant average among 35 other Dysphagia trials with a reported enrollment target (71% lower).
The record links to 1 condition, with Dysphagia appearing as the primary indexed condition, and to 2 interventions - of which Mann Assessment of Swallowing Ability (MASA) (dysphagia screening tool) is the first listed.
NCT05603897 reports a single indexed study location in Florida.
Frequently Asked Questions
What is clinical trial NCT05603897 about?
NCT05603897 is a clinical study titled "Non-standardized vs. Standardized Screening for Dysphagia". The purpose of this study is to compare two different screening tests for detecting dysphagia (difficulty swallowing) as well as the risk for aspiration (silent swallowing of liquids/solids into the lungs) in patients after an ischemic stroke (when a blood clot blocks or narrows an artery leading to...
What is the current status of trial NCT05603897?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2024-04-05. Estimated completion is 2026-01-30.
What conditions does trial NCT05603897 study?
This clinical trial studies the following conditions: Dysphagia.
What interventions are being tested in trial NCT05603897?
The interventions under investigation include: Mann Assessment of Swallowing Ability (MASA) (dysphagia screening tool) (OTHER), Non-standardized clinical swallow evaluation (OTHER).
Who is sponsoring clinical trial NCT05603897?
This trial is sponsored by University of Miami, which has 721 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05603897 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Dysphagia
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT05603897's enrollment target sits among peer trials
50 23rd of 35 higher than 9 of 35 other Dysphagia trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Dysphagia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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