- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00651248
Evaluation of Salivary Flow and Buffer Capacity Associated to Aged People's Oral Health
March 31, 2008 updated by: Academia Cearense de Odontologia
The purpose of this study is to identify the relation of the salivary flow and the buffer capacity of the saliva with medicine, buccal discomfort and auto-related illnesses in aged people.
Study Overview
Status
Completed
Conditions
Detailed Description
Study clinical of prevalence.
68 aged, average 70.4 years, SD ± 7.27 represented institution's residents of long permanence.
Questionnaire was applied, organizing the data for Software SPSS version 15.
The test qui-square of Pearson was used, level of significance 5% and reliable interval 95%.
80% presented pH normal.
The salivary Flow: 32.3% very low, 41.2% reduced and 25.5% normal.
30.9% mentioned dry mouth, 22.1% tasting's problems, 17.6% dysphagia and 14.7% burning mouth.
Main systemic illnesses: 48.5% declared cardiovascular problems, 17.6% diabetes and 16.2% osteoporosis.
76.5% used medicine.
There was a significance statistic between medicine taking and dry mouth (p=0.013),
buffer capacity and burning mouth (p=0.019),
salivary flow and medicine taking (p=0.048).
The low salivary flow and the buffer capacity of the saliva influence in the aged people's health condition, as the drugs influence the results.
Study Type
Observational
Enrollment (Actual)
68
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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Ceara
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Fortaleza, Ceara, Brazil
- Instituição de Longa Permanência Lar Torres de Melo
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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
58 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
68 aged, average 70.4 years, SD ± 7.27 represented institution's residents of long permanence.
Description
Inclusion Criteria:
- aged people with 60 years old or more,
- ills or not,
- able to realize tests
- people who want to participate of research
Exclusion Criteria:
- people less 60 years old
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
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Maria VL Saintrain, doutor, Universidade de Fortaleza
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
September 1, 2006
Study Completion (Actual)
August 1, 2007
Study Registration Dates
First Submitted
March 31, 2008
First Submitted That Met QC Criteria
March 31, 2008
First Posted (Estimate)
April 2, 2008
Study Record Updates
Last Update Posted (Estimate)
April 2, 2008
Last Update Submitted That Met QC Criteria
March 31, 2008
Last Verified
March 1, 2008
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- renatago
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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