Self Assembling Peptide P11-4 in Patients With Early Occlusal Carious Lesions

Dental Caries Clinical Trial

Official title:

Effect of Self Assembling Peptide P11-4 in Patients With Early Occlusal Carious Lesions: A Mono-centre, Controlled, Single-blinded, Randomised Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02724592
• Other study ID #: BB001/13
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: February 2013
• Est. completion date: October 2014

Study information

• Verified date: March 2021
• Source: University Medicine Greifswald
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Objectives: Occlusal surfaces of erupting permanent molars are highly prone to caries. Self-assembling peptide (P11-4) has proven to enhance biomimetic mineralization of early carious lesions. Aim of this study was to evaluate safety, clinical applicability and effect of using P11-4 (Curodont™ Repair) in non-invasive treatment of early occlusal lesions.

Methods: 70 patients with active early occlusal lesions (ICDAS-II:1-3) on first or second permanent molars at eruption will be allocated in this randomized, controlled, single blinded study to test (Curodont™ Repair+Duraphat®) or control (Duraphat®) groups.

Description:

Objectives: Occlusal surfaces of erupting permanent molars are high prone to caries. Self-assembling peptide (P11-4) has proven to enhance biomimetic mineralization of early carious lesions. Aim of this study was to evaluate safety, clinical applicability and effect of using P11-4 (Curodont™ Repair) in non-invasive treatment of early occlusal lesions.

Methods: 70 patients with active early occlusal lesions (ICDAS-II:1-3) on first or second permanent molars at eruption will be allocated in this randomized, controlled, single blinded study to test (Curodont™ Repair+Duraphat®) or control (Duraphat®) groups. Safety and applicability will be evaluated using dentist's/patient's questionnaires about adverse events, difficulties of application and satisfaction with procedure. Lesions will be assessed at baseline and recalls after 3 and 6 months regarding caries activity, clinical status (ICDAS-II) and with Diagnodent®. The Visual Analog Scale (VAS) of regression and of lesion size in addition to the Global Impression of Change Questionnaire will also be assessed. At every recall, fluoride varnish will be applied on lesions and patients received oral health instructions.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 70
• Est. completion date: October 2014
• Est. primary completion date: April 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 5 Years and older

Eligibility

Inclusion Criteria:

• Early occlusal carious lesions (without cavity) on permanent molar "6" or "7" at eruption which does not require an invasive treatment

• Age = 5 years

• Size and form of the lesions: the lesions 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

Related Conditions & MeSH terms

• Dental Caries

Intervention

Device:
• self assembling peptide P11-4 (Curodont™ Repair)
Applying of self assembling peptide P11-4 (Curodont™ Repair) on teeth with initial caries lesions
• fluoride varnish (Duraphat®)
Applying fluoride varnish (Duraphat®) on teeth with initial caries lesions

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University Medicine Greifswald

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Caries Activity and Progression Assessment Using LASER Fluorescence Readings by Diagnodent® Device.	Evaluation of the additional therapeutic benefit of Curodont™ compared to fluoride varnish (Duraphat®) alone on early occlusal carious lesions using LASER "Light Amplification by Stimulated Emission of Radiation" fluorescence readings by Diagnodent® device.; Diagnodent® device measures the caries activity using LASER fluorescence of bacterial secretions in the caries lesion. The readings range from 0 to 99; 0 means no bacterial activity in the carious lesion whereas 99 refers to high bacterial and caries activity.; Effect via the changes in LASER fluorescence readings between Baseline and 6-months recall (Change = Baseline value - 6 months value). Higher positive change value means caries regression, whereas lower positive or negative change value refers to caries progression.	6 months
Secondary	Visual Analog Scale of Lesion Progression (VAS)	Visual Analog Scale of lesion progression (VAS), Effect via t test between Baseline and 6-months recall VAS values range from -100 % to +100 %. The value of -100 means that the carious lesion is strongly remineralising, the value of 0 means that the lesion is arrested, and the value of +100 means that the lesion is strongly progressing.	6 months
Secondary	ICDAS Classification Index	Number of patients who have improvement on the ICDAS classification index (International Caries Detection and Assessment System), changes from Baseline to 6-months recall.; This carries clinical index range from 0 to 6. The values mean: 0 No evidence of caries; Initial caries; Distinct visual change in enamel; Localised enamel breakdown due to caries with no visible dentine; Underlying dark shadow from dentine; Distinct cavity with visible dentine; Extensive distinct cavity with visible dentine. During the study, a change from level to lower level number (e.g. from 2 to 1) in patients means that the carious lesion is regressed.	6 months
Secondary	Caries Activity Assessment According to Nyvad Criteria	Caries activity assessment according to Nyvad criteria, number of participants still have active lesions overall study.; This assessment includes two clinical judgment inserts: active lesion or inactive lesion basing on visual-tactile surface characteristics of the caries lesions such as integrity, texture, translucency/opacity, lesion location, and surface color.; During the study, an alteration from active lesion to in active lesion means an improvement.	6 months