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Preventive Treatment Approach of Early Caries Lesions With Contemporary Methods of Remineralization

Primary Purpose

Tooth Decay

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Fluoride Varnish
Curodont Repair
Curodont Protect
Sponsored by
University Dentistry Clinical Center of Kosovo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tooth Decay

Eligibility Criteria

6 Years - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Early occlusal carious lesion which does not require an invasive treatment (ICDAS-II scores: 2 and 3)
  • Size and form of the lesion: the lesion must both be fully visible and assessable and accessible
  • Willing and able to attend the on-study visits and to observe good oral hygiene throughout the study
  • Written informed consent before participation in the study

Exclusion Criteria:

  • Evidence of tooth Erosion
  • Fluoride varnish application < 3 months prior to study treatment
  • History of head and neck illnesses (e.g. head/neck cancer)
  • Any pathology or concomitant medication affecting salivary flow or dry mouth
  • Any metabolic disorders affecting bone turnover
  • Concurrent participation in another clinical trial

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Active Comparator

    Experimental

    Experimental

    Arm Label

    Control

    Test1

    Test2

    Arm Description

    Fluoride Varnish (Fluor Protector S; Ivoclar, 7'700 ppm F-) application at Day 0 and Day180. => Group: Fluoride Varnish

    Single application of Curodont Repair (P11-4) at Day 0 followed by a Fluoride Varnish (Fluor Protector S; Ivoclar, 7'700 ppm F-) application. Another fluoride Varnish application at Day180. => Group: Curodont Repair + Fluoride Varnish

    Single application of Curodont Repair (P11-4) at Day 0. Curodont Protect (tooth gel containing P11-4 matrix) is handed out and subjects are asked to apply it 2x weekly at home after regular teeth cleaning in the evening for the whole study period (Day 360). => Group: Curodont Repair + Curodont Protect

    Outcomes

    Primary Outcome Measures

    Mean of values measured by Diagnodent(TM) (fluorescence measurement device for carious lesions) for each study group
    Diagnodent values for fissure caries: 0-5: no demineralization, sound. 6-14: outer enamel demineralization. 15-20: inner enamel demineralization. 21-99: dentine demineralization.

    Secondary Outcome Measures

    Mean of values measured by Diagnodent(TM) (fluorescence measurement device for carious lesions) for each study group
    Diagnodent values for fissure caries: 0-5: no demineralization, sound. 6-14: outer enamel demineralization. 15-20: inner enamel demineralization. 21-99: dentine demineralization.
    Frequency of change in ICDAS-II (International caries detection and assessment system) codes for each study group
    Code 0: Sound tooth surface, no evidence of caries after prolonged air drying (5 sec). Code 1: First visual change in enamel. Code 2: Distinct visual change in enamel. Code 3: Localized enamel breakdown due to caries with no visible dentine or underlying shadow. Code 4: Underlying dark shadow from dentine with or without enamel breakdown. Code 5: Distinct cavity with visible dentine. Code 6: Extensive distinct cavity with visible dentine (involving more than half of the dentine).
    Frequency of change in caries lesion activity and severity assessed by Nyvad criteria for each study group
    Score 0: Sound. Score 1: Active caries - intact surface. Score 2: Active caries - surface discontinuity. Score 3: Active caries - cavity. Score 4: Inactive caries - intact surface. Score 5: Inactive caries - surface discontinuity. Score 6: Inactive caries - cavity.
    Mean of VAS values (Visual analogue scale) for each study group
    Range: from -50 (strongly remineralizing) to +50 (stronlgy progressing)
    Frequency of Evaluation Outcome of Global Impression of Change Questionnaire for each study group
    Investigator Questionnaire: evaluation ranging from "very much worse" to "very much better"; 7-point scale

    Full Information

    First Posted
    December 6, 2018
    Last Updated
    December 17, 2018
    Sponsor
    University Dentistry Clinical Center of Kosovo
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03780270
    Brief Title
    Preventive Treatment Approach of Early Caries Lesions With Contemporary Methods of Remineralization
    Official Title
    Preventive Treatment Approach of Early Caries Lesions With Contemporary Methods of Remineralization
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    June 16, 2014 (Actual)
    Primary Completion Date
    December 31, 2016 (Actual)
    Study Completion Date
    December 31, 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University Dentistry Clinical Center of Kosovo

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this study is to evaluate the additional therapeutic benefit of Curodont Repair for the treatment early occlusal carious lesions on permanent teeth in children compared fluoride varnish alone the tooth gel Curodont Protect when using it after Curodont Repair instead of fluoride varnish
    Detailed Description
    Objectives: The purpose of this study is to evaluate the additional therapeutic benefit of Curodont Repair for the treatment early occlusal carious lesions on permanent teeth in children compared fluoride varnish alone the tooth gel Curodont Protect when using it after Curodont Repair instead of fluoride varnish Methods: 90 patients with early occlusal lesions (ICDAS-II:2-3) on permanent molars and pre-molars will be allocated in this randomized, controlled, single blinded study to one of the two test groups (Test1: Curodont™ Repair+Fluoride Varnish; Test2: Curodont Repair+Curodont Protect) or control (Fluoride Varnish) group. Lesions will be assessed at baseline and recalls after 3, 6 and 12 months regarding caries activity (Nyvad), clinical status (ICDAS-II) and with Diagnodent®. Visual Analog Scale (VAS) in addition to the Global Impression of Change Questionnaire will also be used for the evaluation of the outcome.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Tooth Decay

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    90 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Control
    Arm Type
    Active Comparator
    Arm Description
    Fluoride Varnish (Fluor Protector S; Ivoclar, 7'700 ppm F-) application at Day 0 and Day180. => Group: Fluoride Varnish
    Arm Title
    Test1
    Arm Type
    Experimental
    Arm Description
    Single application of Curodont Repair (P11-4) at Day 0 followed by a Fluoride Varnish (Fluor Protector S; Ivoclar, 7'700 ppm F-) application. Another fluoride Varnish application at Day180. => Group: Curodont Repair + Fluoride Varnish
    Arm Title
    Test2
    Arm Type
    Experimental
    Arm Description
    Single application of Curodont Repair (P11-4) at Day 0. Curodont Protect (tooth gel containing P11-4 matrix) is handed out and subjects are asked to apply it 2x weekly at home after regular teeth cleaning in the evening for the whole study period (Day 360). => Group: Curodont Repair + Curodont Protect
    Intervention Type
    Device
    Intervention Name(s)
    Fluoride Varnish
    Intervention Description
    Fluor Protector S (Ivoclar, 7'700 ppm F-)
    Intervention Type
    Device
    Intervention Name(s)
    Curodont Repair
    Intervention Description
    P11-4 (monomeric peptide) - for professional use
    Intervention Type
    Device
    Intervention Name(s)
    Curodont Protect
    Intervention Description
    Tooth gel (containing P11-4 assembled to a fibrillary matrix) - for home use (OTC)
    Primary Outcome Measure Information:
    Title
    Mean of values measured by Diagnodent(TM) (fluorescence measurement device for carious lesions) for each study group
    Description
    Diagnodent values for fissure caries: 0-5: no demineralization, sound. 6-14: outer enamel demineralization. 15-20: inner enamel demineralization. 21-99: dentine demineralization.
    Time Frame
    Day 180
    Secondary Outcome Measure Information:
    Title
    Mean of values measured by Diagnodent(TM) (fluorescence measurement device for carious lesions) for each study group
    Description
    Diagnodent values for fissure caries: 0-5: no demineralization, sound. 6-14: outer enamel demineralization. 15-20: inner enamel demineralization. 21-99: dentine demineralization.
    Time Frame
    Day 90 and Day 360
    Title
    Frequency of change in ICDAS-II (International caries detection and assessment system) codes for each study group
    Description
    Code 0: Sound tooth surface, no evidence of caries after prolonged air drying (5 sec). Code 1: First visual change in enamel. Code 2: Distinct visual change in enamel. Code 3: Localized enamel breakdown due to caries with no visible dentine or underlying shadow. Code 4: Underlying dark shadow from dentine with or without enamel breakdown. Code 5: Distinct cavity with visible dentine. Code 6: Extensive distinct cavity with visible dentine (involving more than half of the dentine).
    Time Frame
    Day 90, Day 180, Day 360
    Title
    Frequency of change in caries lesion activity and severity assessed by Nyvad criteria for each study group
    Description
    Score 0: Sound. Score 1: Active caries - intact surface. Score 2: Active caries - surface discontinuity. Score 3: Active caries - cavity. Score 4: Inactive caries - intact surface. Score 5: Inactive caries - surface discontinuity. Score 6: Inactive caries - cavity.
    Time Frame
    Day 90, Day 180, Day 360
    Title
    Mean of VAS values (Visual analogue scale) for each study group
    Description
    Range: from -50 (strongly remineralizing) to +50 (stronlgy progressing)
    Time Frame
    Day 90, Day 180, Day 360
    Title
    Frequency of Evaluation Outcome of Global Impression of Change Questionnaire for each study group
    Description
    Investigator Questionnaire: evaluation ranging from "very much worse" to "very much better"; 7-point scale
    Time Frame
    Day 90, Day 180, Day 360

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    6 Years
    Maximum Age & Unit of Time
    15 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Early occlusal carious lesion which does not require an invasive treatment (ICDAS-II scores: 2 and 3) Size and form of the lesion: the lesion must both be fully visible and assessable and accessible Willing and able to attend the on-study visits and to observe good oral hygiene throughout the study Written informed consent before participation in the study Exclusion Criteria: Evidence of tooth Erosion Fluoride varnish application < 3 months prior to study treatment History of head and neck illnesses (e.g. head/neck cancer) Any pathology or concomitant medication affecting salivary flow or dry mouth Any metabolic disorders affecting bone turnover Concurrent participation in another clinical trial
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Dafina Doberdoli, Dr.
    Organizational Affiliation
    University Dentistry Clinical Center of Kosovo
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Preventive Treatment Approach of Early Caries Lesions With Contemporary Methods of Remineralization

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