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Probiotics in Special Needs Patients at High Risk for Tooth Decay: a Randomized Controlled Trial.

Primary Purpose

Tooth Decay, Intellectual Disability, Caries,Dental

Status
Not yet recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Test Group
Positive Control
Negative Control
Sponsored by
G. d'Annunzio University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tooth Decay focused on measuring caries;, tooth decay, intellectual disability, probiotics, lactobacillus rhamnosus, lactobacillus plantarum, pH

Eligibility Criteria

10 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: individuals with intellectual disability in presence of gingivitis in 1 quadrant at least and 1 decayed tooth at least, and improper oral hygiene routine. Exclusion Criteria: individuals without intellectual disability or with the condition in absence of gingivitis, decayed teeth and improper oral hygiene routine.

Sites / Locations

  • University G. d'Annunzio

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Other

Arm Label

Test Group

Positive Control

Negative Control

Arm Description

Subjects who will receive orally administred probiotics based on L. rhamnosus and L. plantarum for 90 days in adjunction to the instruction of their care-giver regarding oral hygiene procedures.

Subjects who will receive orally administred probiotics based on placebo for 90 days in adjunction to the instruction of their care-giver regarding oral hygiene procedures.

Subjects who will receive esclusively the instruction of their care-giver regarding oral hygiene procedures.

Outcomes

Primary Outcome Measures

Reduction of clinical dicotomic indexes for gingivitis
Gingivitis will be recorded for each quadrant as present/absent taking into account the classical flogistic signs.

Secondary Outcome Measures

management of salivary pH
Salivary pH will be recorded via digital pHmeter 3/times for each time-point in order to minimaze the error of registration.

Full Information

First Posted
September 26, 2023
Last Updated
September 30, 2023
Sponsor
G. d'Annunzio University
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1. Study Identification

Unique Protocol Identification Number
NCT06063239
Brief Title
Probiotics in Special Needs Patients at High Risk for Tooth Decay: a Randomized Controlled Trial.
Official Title
Probiotics in Special Needs Patients at High Risk for Tooth Decay: a Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 1, 2023 (Anticipated)
Primary Completion Date
March 1, 2024 (Anticipated)
Study Completion Date
May 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
G. d'Annunzio University

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 goal of this randomized clinical trial is to test the effect orally administration of Probiotics based on Lactobacillus rhamnosus LR04 and Lactobacillus plantarum LP14 as adjuvant in caries prevention in subjects who can not properly perform oral hygiene procedures. The main questions it aims to answer are: QUESTION 1: orally administered probiotics based on the previous strains could represent a useful tool in support of special needs patients in tooth decay prevention? QUESTION 2: orally administered probiotics based on the previous strains could ameliorate salivary pH management? Partecipants in the test group will take the test probiotic for 90 days in adjunction of the routinary oral hygiene procedures. Partecipants in the positive controlled group will take the placebo for 90 days in adjunction of the routinary oral hygiene procedures. Partecipants in the negative control group will perform only the routinary oral hygiene procedures. Researchers will compare 3 groups to see if orally administered probiotics based on L. rhamnosus and L. plantarum may help in the management of clinical status and salivary pH levels.
Detailed Description
Recent literature has highlighted how patients' oral health is closely linked to the presence of intellectual and developmental disabilities (IDD). It has in fact been found that in patients with IDD the level of oral health tends to be lower than in subjects without IDD, and how this has an influence on the general state of health. A key role appears to be played by caregivers, who carry out the delicate task of maintaining an adequate level of oral hygiene. Among various aspects, daily oral hygiene maneuvers were considered as a key intervention in maintaining good health. In this regard, it is worth remembering that a study conducted in 1990 on caregivers demonstrated how, despite knowing the characteristics of the healthy appearance of the tissues supporting the dental elements, not everyone knew how this was closely related to the oral hygiene. Likewise, the study by Kilian and collaborators demonstrated how the maintenance of an oral microbiota that promotes oral health is not only desirable, but also possible. Given that the implementation of correct home hygiene represents a cornerstone in the management of general well-being, we decided to evaluate whether a formulation that allows the strengthening of bacterial populations competitive with respect to cariogenic populations could be significantly useful for the maintenance of these patients. Inclusion criteria: adult and minor special needs patients belonging to the University Dental Clinic of Chieti. Presence of motor and/or cognitive difficulties in carrying out oral hygiene maneuvers at home. Exclusion criteria: special needs patients with effective home hygiene. Minimum sample size: Calculation of sample size (Alpha = 0.05; Power = 95%) for 3 independent study groups, and a continuous primary endpoint. Sample size = Z2 (1-alpha/2) p (1-p) / d2 Where Z(1-alpha/2) is the standard variate corresponding to 1.96 at 5% type 1 error, p is the expected proportion in the population expressed in decimals based on previous studies and d is the confidence level decided by the researcher expressed in decimal. 20 patients are required per group, for a total of 60 patients. To these patients, the dropout percentage of 10% must be added, so the total is 70 patients. BASELINE - T0. Signature of informed consent. Completion of a specific questionnaire regarding consumption of simple sugars and initial home oral hygiene procedures. Oral cavity inspection with registration of gingivitis according to dichotomous qualitative indices by quadrants.Recording of specific parameters: Salivary pH via GEASS® pH meter. DMFT (Decayed Missing Filled Teeth). Random placement of the patient in the test, positive or negative control group. TEST: instruction of the subject and/or caregiver in home oral hygiene 2/day + oeally administred probiotic based on L. plantarum and L. rhamnosus for 90 days. POSITIVE CONTROL: instruction of the subject and/or caregiver in home oral hygiene 2/day + orally administred placebo. NEGATIVE CONTROL: instruction of the subject and/or caregiver for home oral hygiene procedures 2/day. T1 - AFTER 3 MONTHS FROM T0. Oral cavity inspection with recording of gingivitis according to dichotomous qualitative indices by quadrants. Recording of pH and DMFT. Randomization. The treatment that is due to the individual patient is kept in sequentially numbered, opaque and sealed envelopes (SNOSE Sequentially Numbered, Opaque, Sealed Envelopes). The products used for both the test and the controls will be supplied in anonymous tubes so that neither the patient nor the investigator will be aware of them. Statistical analysis: Developed by trusted bioinformatics group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tooth Decay, Intellectual Disability, Caries,Dental
Keywords
caries;, tooth decay, intellectual disability, probiotics, lactobacillus rhamnosus, lactobacillus plantarum, pH

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
SNOSE Sequentially Numbered, Opaque, Sealed Envelopes
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Test Group
Arm Type
Experimental
Arm Description
Subjects who will receive orally administred probiotics based on L. rhamnosus and L. plantarum for 90 days in adjunction to the instruction of their care-giver regarding oral hygiene procedures.
Arm Title
Positive Control
Arm Type
Active Comparator
Arm Description
Subjects who will receive orally administred probiotics based on placebo for 90 days in adjunction to the instruction of their care-giver regarding oral hygiene procedures.
Arm Title
Negative Control
Arm Type
Other
Arm Description
Subjects who will receive esclusively the instruction of their care-giver regarding oral hygiene procedures.
Intervention Type
Other
Intervention Name(s)
Test Group
Intervention Description
Subjects will receive orally administred probiotics based on L. plantarum and L. rhamnosus for 90 days
Intervention Type
Other
Intervention Name(s)
Positive Control
Intervention Description
Subjects will receive orally administred probiotics based on placebo 90 days
Intervention Type
Other
Intervention Name(s)
Negative Control
Intervention Description
Subjects will receive esclusively instruction to perform oral hygiene procedures properly.
Primary Outcome Measure Information:
Title
Reduction of clinical dicotomic indexes for gingivitis
Description
Gingivitis will be recorded for each quadrant as present/absent taking into account the classical flogistic signs.
Time Frame
From enrollement to the end of treatment at 3 months.
Secondary Outcome Measure Information:
Title
management of salivary pH
Description
Salivary pH will be recorded via digital pHmeter 3/times for each time-point in order to minimaze the error of registration.
Time Frame
From enrollement to the end of treatment at 3 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: individuals with intellectual disability in presence of gingivitis in 1 quadrant at least and 1 decayed tooth at least, and improper oral hygiene routine. Exclusion Criteria: individuals without intellectual disability or with the condition in absence of gingivitis, decayed teeth and improper oral hygiene routine.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marco Dolci, MD DDS PHD
Phone
+393281665925
Email
marco.dolci@unich.it
First Name & Middle Initial & Last Name or Official Title & Degree
Silvia D'Agostino, DDS PHD
Phone
+393281665925
Email
silvia.dagostino@unich.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marco Dolci, MD DDS PHD
Organizational Affiliation
University G. d'Annunzio of Chieti
Official's Role
Principal Investigator
Facility Information:
Facility Name
University G. d'Annunzio
City
Chieti
ZIP/Postal Code
66100
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marco Dolci, MD DDS PHD
Phone
+393281665925
Email
marco.dolci@unich.it
First Name & Middle Initial & Last Name & Degree
Silvia D'Agostino, DDS PHD
Phone
+393930246351
Email
silvia.dagostino@unich.it

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
A decision regarding IPD sharing has not been made yet because a dedicated website is not available at the momente.
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Probiotics in Special Needs Patients at High Risk for Tooth Decay: a Randomized Controlled Trial.

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