Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01305265 · ClinicalTrials.gov registry record · NA
Post-operative Sore Throat as Determined by Endotracheal Tube Inflation Technique
A NA study, sponsored by University of California, San Francisco.
- Completed
- Registry status
- NA
- Development phase
- 141
- Enrollment target
NCT01305265 is a NA study that has completed, run by University of California, San Francisco. The registered enrollment target is 141 participants.
The verdict
NCT01305265, a NA study, has completed, sponsored by University of California, San Francisco.
- COMPLETED
- Registry status
- NA
- Development phase
- 141 participants
- Enrollment target
Study Summary
The purpose of this study is to test whether the incidence of sore throat and other tracheal co-morbidities such as dysphagia and hoarseness can be lessened by use of a cuff manometer at the beginning of surgery to inflate to the proper pressure compared to the standard technique. The investigators hypothesis is that inflation of the endotracheal balloon using a cuff manometer immediately after intubation will reduce the incidence of sore throat and other tracheal co-morbidities.
Interventions
- DEVICE cuff manometer
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 141 participants |
| Start Date | 2011-11 |
| Est. Completion | 2012-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01305265
The ClinicalTrials.gov registry entry for NCT01305265 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 141 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which cuff manometer is the first listed.
NCT01305265 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01305265 about?
NCT01305265 is a clinical study titled "Post-operative Sore Throat as Determined by Endotracheal Tube Inflation Technique". The purpose of this study is to test whether the incidence of sore throat and other tracheal co-morbidities such as dysphagia and hoarseness can be lessened by use of a cuff manometer at the beginning of surgery to inflate to the proper pressure compared to the standard technique. The investigators...
What is the current status of trial NCT01305265?
This trial is currently completed. It is a NA study. The enrollment target is 141 participants. The study started on 2011-11. Estimated completion is 2012-12.
What interventions are being tested in trial NCT01305265?
The interventions under investigation include: cuff manometer (DEVICE).
Who is sponsoring clinical trial NCT01305265?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.