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Effect of Curodont Repair or Placebo on the Remineralisation in Patients With Class 5 Carious Lesions

NCT02020681 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2019-08-30

No results posted yet for this study

Summary

The purpose of this study is to evaluate the therapeutic benefit of Curodont Repair for the treatment of early buccal carious lesions compared to placebo.

Conditions

  • Dental Caries

Interventions

DEVICE

Curodont Repair

Self-assembling peptide, biomimetic re-mineralisation

OTHER

Placebo

Formulation of Curodont Repair without the peptide P11-4

DEVICE

Fluoride

Single application on day D90

Sponsors & Collaborators

  • Credentis AG

    lead INDUSTRY

Principal Investigators

  • Ivo Krejci, Prof. Dr. · University of Geneva

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
14 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2016-01-31
Completion
2016-01-31

Countries

  • Switzerland

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 NCT02020681 on ClinicalTrials.gov