- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01576926
Evolution of Swallowing in Patients Undergoing Lateral Pharyngoplasty With Preservation Stylopharyngeal Muscle
April 11, 2012 updated by: Jayson mesti, Hospital do Servidor Publico Estadual
Evolution of swallowing in patients undergoing lateral pharyngoplasty with preservation stylopharyngeal muscle.
Study Overview
Status
Completed
Conditions
Detailed Description
refer patients to the side pharyngoplasty with total preservation of stylopharyngeal muscle and evaluate the total recovery time of swallowing, making a daily assessment.
Study Type
Observational
Enrollment (Actual)
1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Sao Paulo, Brazil
- Hospital do Servidor Publico Estadual
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
patients with obstructive sleep apnea, indicating the lateral pharyngeal
Description
Inclusion Criteria:
- patients with obstructive sleep apnea with surgical indication
Exclusion Criteria:
- patients with obstructive sleep apnea without surgical indication
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
---|
surgery
patients with obstructive sleep apnea
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Evolution of swallowing in patients undergoing lateral pharyngoplasty with preservation stylopharyngeal muscle
Time Frame: assess progress daily until the end of swallowing dysphagia during 30 days
|
refer patients with oas to the side faringolastia with total preservation stylopharyngeal muscle and evaluate recovery time of swallowing during 30 days.
|
assess progress daily until the end of swallowing dysphagia during 30 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Evolution of swallowing in patients undergoing lateral pharyngoplasty with preservation stylopharyngeal muscle
Time Frame: assess progress daily until the end of swallowing dysphagia during 30 days
|
refer patients with oas to the side faringolastia with total preservation styleopharingeal muscle and evaluate the total recovery time of swallowing, making a daily assessment.
|
assess progress daily until the end of swallowing dysphagia during 30 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Jayson Mesti, medical, Hopital Do Servidor Público Estadual
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2009
Primary Completion (Actual)
June 1, 2011
Study Completion (Actual)
February 1, 2012
Study Registration Dates
First Submitted
April 9, 2012
First Submitted That Met QC Criteria
April 11, 2012
First Posted (Estimate)
April 13, 2012
Study Record Updates
Last Update Posted (Estimate)
April 13, 2012
Last Update Submitted That Met QC Criteria
April 11, 2012
Last Verified
April 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 116/08
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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