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Dental Erosion in Patients With Gastro-oesophageal Reflux

Dental Erosion in Patients With Gastro-oesophageal Reflux

Status
Suspended
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02775149
Enrollment
30
Registered
2016-05-17
Start date
2016-11-01
Completion date
2021-12-31
Last updated
2020-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Erosion

Brief summary

Not only caries but also exposure to acids can lead to loss of tooth structure. This acid-related tooth structure loss is defined as dental erosion. A relationship between dental erosion and occurence of reflux disease was shown in numerous studies. On the one hand, patients with dental erosions frequently show reflux disease. On the other hand, many - but not all - reflux patients show dental erosions. It is believed that certain salivary parameters might explain, why not all reflux patients alike are affected of dental erosions. The aim of this study is to analyze the relationship and the extent of occurrence of dental erosions and reflux symptoms, including investigation of certain salivary parameters.

Interventions

Collection of saliva samples

OTHERVisual detection of BEWE-index

Visual detection of BEWE-index

Sponsors

University of Göttingen
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients who are treated at the Clinic for Gastroenterology and Gastrointestinal Oncology and have a 24-hours pH monitoring or impedance measurement performed for medical reasons

Exclusion criteria

* Inability to give written consent * Age \<18 years * Intake of proton pump inhibitors (PPIs) if they are not discontinued at least one week before study participation

Design outcomes

Primary

MeasureTime frame
Visual assessment of the BEWE-(basic erosive wear examination)-indexAfter removal of the probe (on second day)

Secondary

MeasureTime frame
Determination of unstimulated and stimulated saliva flow rate (ml/min).While wearing the probe at three time points over 24h: morning, noon, evening
Determination of saliva pH and buffer capacity (mol/L).While wearing the probe at three time points over 24h: morning, noon, evening
Determination of total protein content in saliva (g/L).While wearing the probe at three time points over 24h: morning, noon, evening
Determination inorganic calcium and phosphate in saliva (mmol/L).While wearing the probe at three time points over 24h: morning, noon, evening
Measurement of salivary enzyme activity: Protease, Kollagenase/Gelatinase, Pepsin, Trypsin, and Amylase (U/mL).While wearing the probe at three time points over 24h: morning, noon, evening

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026