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Pilot Study Utilising an Impression Technique to Capture in Vivo Images of Teeth

NCT02676219 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2018-06-08

No results posted yet for this study

Summary

The study design is a randomised, split mouth, blind with respect to study analysts (microscopist, image grader) two treatment clinical study in 10 healthy participants with sound tooth enamel. The study will comprise of a screening visit, pre-baseline visit and 5 subsequent clinic visits. At the screening visit, participants will give consent to participate in the study. Medical history and concomitant medications will be recorded. Eligibility will be determined following an oral soft tissue (OST) examination and an evaluation of dentition exclusions. Two suitable anterior teeth will be identified for study assessments, these teeth must be at least one tooth apart in the mouth. Saliva samples will be collected from the participants at set points during the study to look at any changes in salivary pH.

Conditions

  • Tooth Erosion

Interventions

OTHER

RS01

Oral Care product containing sodium monofluorophosphate and sodium fluoride

OTHER

Water

Sponsors & Collaborators

  • University of Bristol Dental Hospital

    collaborator OTHER

  • Unilever R&D

    lead INDUSTRY

Principal Investigators

  • Nicola X West, BDS · University of Bristol Dental Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-07-01
Primary Completion
2015-09-18
Completion
2015-09-18

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02676219 on ClinicalTrials.gov