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NCT01849679 · ClinicalTrials.gov registry record
Post Extubation Dysphagia
A clinical trial, sponsored by University of Wisconsin, Madison.
- Completed
- Registry status
- 71
- Enrollment target
NCT01849679 is a clinical trial that has completed, run by University of Wisconsin, Madison. The registered enrollment target is 71 participants.
The verdict
NCT01849679 has completed, sponsored by University of Wisconsin, Madison.
- COMPLETED
- Registry status
- 71 participants
- Enrollment target
Study Summary
The investigators hypothesize that aspiration will be more prevalent at two to four hours post-extubation but will resolve in the majority of patients by 24 to 26 hours post-extubation. The purpose of the research is to investigate whether there is a difference in swallow function two to four hours after extubation (removal of breathing tube) compared to 24 hours after extubation. This information will help healthcare providers decide if it is necessary for people to wait 24 hours after extubation before they start eating and drinking.
Interventions
- OTHER Evaluation of Swallowing
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 71 participants |
| Start Date | 2013-03 |
| Est. Completion | 2016-02 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01849679
The ClinicalTrials.gov registry entry for NCT01849679 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 71 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Wisconsin, Madison, which has 1,039 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Evaluation of Swallowing is the first listed.
NCT01849679 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01849679 about?
NCT01849679 is a clinical study titled "Post Extubation Dysphagia". The investigators hypothesize that aspiration will be more prevalent at two to four hours post-extubation but will resolve in the majority of patients by 24 to 26 hours post-extubation. The purpose of the research is to investigate whether there is a difference in swallow function two to four hours...
What is the current status of trial NCT01849679?
This trial is currently completed. The enrollment target is 71 participants. The study started on 2013-03. Estimated completion is 2016-02.
What interventions are being tested in trial NCT01849679?
The interventions under investigation include: Evaluation of Swallowing (OTHER).
Who is sponsoring clinical trial NCT01849679?
This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.
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