Relationship and Pathophysiology of Gastroesophageal Reflux and Dental/Periodontal Disease
Completed
Conditions studied: Gastroesophageal Reflux, Dental Erosion
In brief
This study investigates the prevalence and pathophysiology of dental and periodontal involvement in pediatric patients with symptomatic or asymptomatic gastroesophageal reflux (GER) or gastroesophageal reflux disease (GERD). Primary objectives are to compare the prevalence of oral disease in children with and without a diagnosis or symptoms/signs of GERD in a cross-sectional study. Secondary objectives are to examine factors that might lead to the pathogenesis of the dental and periodontal lesions observed in this group of subjects. The primary hypothesis is to prove that children aged 10-18 years diagnosed with or having symptoms or signs of GERD have a significantly higher amount of dental erosions in comparison to a matched control group. Secondary hypotheses are that children aged 10 - 18 years diagnosed with or having signs of GER have higher DMFS (Decayed, Missing, Filled permanent tooth Surfaces) rates, higher SBI (Sulcus Bleeding Index) rates, worse Periodontal status, and lower saliva buffering capacity.
Key facts
- Study ID
- NCT01167543
- Run by
- University of California, San Francisco
- People needed
- 79
- Starts
- 2005-09-01
- Expected to finish
- 2008-11-01
- Last updated by the study team
- 2010-07-22
Who can join
Age: 9 and older, up to 18. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Ages 9.0 to 18.0 years, of either gender
- Able to give verbal / written assent / consent themselves and/or informed consent from a parent/guardian
- Willing to comply with all study procedures and protocols,
- Willing to get dental photographs and impressions taken
- Willing to sign the "Authorization for Release of Personal Health Information and Use of Personally Unidentified Study Data for Research" form
You may not qualify if…
- Subjects suffering from systemic diseases, significant past or medical history with conditions that may affect oral health or oral flora (i.e. diabetes, HIV, heart conditions that require antibiotic prophylaxis)
- Other conditions that may decrease the likelihood of adhering to study protocol,
- Subjects who will leave the area and are unable to complete the study.
Where it is running
- University of California, San Francisco Dental School — San Francisco, California, United States
Full record on ClinicalTrials.gov
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