- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01275079
Change of Nasalance After Tonsillectomy in Thai Adult
January 11, 2011 updated by: Chulalongkorn University
The purpose of this study is to analyze the change of nasalance after tonsillectomy in Thai adults.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Permpoon Piyaman, MD
- Phone Number: +6622564103
- Email: jawmor@hotmail.com
Study Contact Backup
- Name: Napadon Tangjaturonrasme, ENT
- Phone Number: +6622564103
- Email: napadont@yahoo.com
Study Locations
-
-
-
Bangkok, Thailand, 10330
- Recruiting
- Department of Otolaryngology, Faculty of Medicine, Chulalongkorn University
-
Contact:
- Permpoon Piyaman, MD
-
Contact:
- Napadon Tangjaturonrasme
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Thai adults who were performed tonsillectomy
Description
Inclusion Criteria:
- Thai adults age over 18 years who were perform bilateral tonsillectomy
- The pathological are not malignancy
Exclusion Criteria:
- Craniofacial anomalies
- Neurological problems
- History of Peritonsillar abscess
- Performed other operation beside tonsillectomy
- Can't read Thais
- Visual problem that effect reading
- Nasal disease that cause nasal obstruction
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
- Observational Models: Cohort
- Time Perspectives: Prospective
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Permpoon Piyaman, MD, Department of Otolaryngology, Faculty of Medicine, Chulalongkorn University
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
January 1, 2011
Primary Completion (Anticipated)
October 1, 2011
Study Completion (Anticipated)
December 1, 2011
Study Registration Dates
First Submitted
November 26, 2010
First Submitted That Met QC Criteria
January 11, 2011
First Posted (Estimate)
January 12, 2011
Study Record Updates
Last Update Posted (Estimate)
January 12, 2011
Last Update Submitted That Met QC Criteria
January 11, 2011
Last Verified
January 1, 2011
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Resident_Permpoon
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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