Domiciliary Management of Dental Erosion in Patients With GERD With Biomimetic Hydroxyapatite

University of Pavia

Status: Completed

Conditions: Dental Erosion; Gastro Esophageal Reflux

Treatments: Other: Domiciliary use of Biorepair Total Protection + Biorepair Shock Treatment; Other: Biorepair Total Protection

Study type: Interventional

Funder types: Other

Identifiers

NCT05371717

2022-GASTRO

Details and patient eligibility

About

The aim of the present study is to evaluate dental erosion in patients with gastroesophageal reflux disease (GERD).

Patients consenting to participate to the study will undergo periodontal evaluation at the baseline. Then, professional dental hygiene will be performed. Patients will be randomly assigned to:

• Trial group: home oral hygiene with Biorepair Total Protection + Biorepair Shock Treatment twice a day
• Control group: home oral hygiene with Biorepair Total Protection Patients will be evaluated after 1, 3, 6, 9 and 12 months from baseline.

Full description

The aim of the present study is to evaluate dental erosion in patients with gastroesophageal reflux disease (GERD).

Patients consenting to participate to the study will undergo periodontal evaluation at the baseline. Then, professional dental hygiene will be performed. Patients will be randomly assigned to:

• Trial group: home oral hygiene with Biorepair Total Protection + Biorepair Shock Treatment twice a day
• Control group: home oral hygiene with Biorepair Total Protection Patients will be evaluated after 1, 3, 6, 9 and 12 months from baseline.

Enrollment: 30 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• patients with dental erosion
• no proton pumps before pH examination

Exclusion criteria

• no dental erosion
• neurological and psychiatric diseases;
• pregnant and/or breastfeeding women;
• patients with poor compliance.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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30 participants in 2 patient groups

Trial Group

Experimental group

Description:

Domiciliary use of Biorepair Total Protection + Biorepair Shock Treatment application

Treatment:

Other: Domiciliary use of Biorepair Total Protection + Biorepair Shock Treatment

Control group

Active Comparator group

Description:

Domiciliary use of Biorepair Total Protection

Treatment:

Other: Biorepair Total Protection