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Carnosine Supplementation on Quantity/Quality of Oral Salivae. (PHoral)

Primary Purpose

Oral Diseases

Status
Not yet recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
400 mg mucoadhesive oral tablet
placebo mucoadhesive oral tablet
Sponsored by
University of Milan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Oral Diseases focused on measuring dental erosions, caries, périodontopathies

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria for Oral Diseased subjects:

  • dental erosions (De)
  • caries (Ca)
  • périodontopathies (Pe)

Exclusion Criteria for both:

  • allergies/intolerances to the consumption of Carnosine
  • taking other food supplements
  • any type of drug treatment (interview)
  • smoking
  • pregnancy/lactation
  • any systemic diseases such as cardiovascular and respiratory, diabetes mellitus, HIV infection, or inflammatory conditions causing non-plaque dependent OD.

Sites / Locations

  • Department of Biomedical, Surgical, and Dental Sciences, Istituto Stomatologico Italiano, Aesthetic Dentistry, School of Dentistry, University of Milan, Milan, Italy.

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Experimental

Placebo Comparator

Experimental

Arm Label

Controls subjects placebo

Controls subjects active Treatment

Diseased subjects placebo

Diseased subjects active Treatment

Arm Description

Placebo mucoadhesive oral tablet

AqualiefTM 400 mg mucoadhesive oral tablet

Placebo mucoadhesive oral tablet

AqualiefTM 400 mg mucoadhesive oral tablet

Outcomes

Primary Outcome Measures

Effects on oral pH.
Any change of oral pH from basal.
Saliva Production unstimulated.
Change of oral saliva production, unstimulated.
Saliva Production stimulated.
Change of oral saliva production, stimulated.

Secondary Outcome Measures

Full Information

First Posted
February 26, 2020
Last Updated
May 17, 2022
Sponsor
University of Milan
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1. Study Identification

Unique Protocol Identification Number
NCT04295525
Brief Title
Carnosine Supplementation on Quantity/Quality of Oral Salivae.
Acronym
PHoral
Official Title
PHoral: Effects of Carnosine Supplementation on Quantity/Quality of Oral Salivae in Healthy Volunteer and in Subjects Affected by Common Oral Pathologies.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2022 (Anticipated)
Primary Completion Date
December 1, 2022 (Anticipated)
Study Completion Date
December 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Milan

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 aim of this study is to elucidate the mutual relationship between salivae characteristics and oral microbiome and to compare them with common oral disease; furthermore, by using specific bioinformatic tools to analyse the data, the potentials of Carnosine in preventing/treating oral diseases and its mechanism of action will be addressed by using quantitative proteomics.
Detailed Description
The pH of the oral cavity is a synthetic parameter that underlies a multifactorial process of continuous adjustment that includes the effect of salivae as a buffer and the contribution of the oral cavity microbiome. In some diseases of the oral cavity an alteration of these adjustment mechanisms is supposed to alter the normal flow of salivae and, consequently, the pH and the oral microbiome with the expansion of potentially pathogenic strains such as e.g. streptococcus viridans. Carnosine (Car) is an endogenous dipeptide, composed of β-alanine and L-histidine, that was originally discovered in larger amounts in skeletal muscle of some vertebrates, including humans, showing a greater dependence on non-oxidative forms of energy metabolism. This peculiar association with muscular tissue and its pH-buffering properties has led to associate Car with the intracellular acid-base homeostasis of muscles. More recently, the physiological role of Car has been expanded beyond the intracellular buffering properties, supporting a role in sarcoplasmic Ca2+ regulation and neutralisation of reactive oxygen species (ROS). It is well known that ROS induce the formation of reactive electrophilic carbonyl species by reacting with lipids and sugars which, in turn, react with proteins forming irreversible adducts (AGEs, ALEs and EAGLEs) and cross-links that may affect the cardiovascular wall matrix that becomes less distensible, especially during the ageing process and/or diseases. Thus it is thought that Car and, indeed, other histidine-containing peptide (HCD), may prevent chronic diseases via their anti-inflammatory, anti-oxidative, anti-glycating, anti-ischaemic and chelating properties. Furthermore, the localisation of Car in other tissues such as brain, olfactory bulb, heart, stomach, pancreas, kidney has suggested further potential uses in preventing e.g. neurodegenerative disorder and cognitive function or the development of type II diabetes. The oral microbiome (OM) is a relevant part of the whole human MO since it contains several different niches, with distinct microbial communities, colonising the oral cavity (OC), including not only bacteria but also fungi, viruses, archaea and protozoa. These communities form a complex ecological system that influences OC and systemic health. Indeed the prevalent oral diseases (OD), namely dental caries and periodontal diseases, are believed to be microbiota-related. Furthermore, several evidences support the theory that many systemic diseases are associated with an altered OM, among these the most frequently associated diseases are metabolic, such as diabetes, cardiovascular and oncological ones. For their prevalence worldwide, among OD, periodontal infection, including gingivitis and chronic periodontitis, is possibly the most prevalent human microbial diseases (HMD). In order to protect the OC from HMD, in the present project Car has been chosen as a possible preventive and/or therapeutic principle for its aforementioned multiple biological effects. Thus the safety and efficacy of AqualiefTM (Metis Healthcare s.r.l., Milano, Italy) a 400 mg mucoadhesive oral tablet (13 x 4 mm), that recognise Car as main ingredient, will be tested on healthy volunteer and in subjects affected by common OD. The main objectives of this protocol are to estimate the quantity/quality of oral salivae and OM in healthy volunteer and in patients affected by common OD, before and after 7 days of treatment with AqualiefTM, 1 tablet twice. The characteristics of oral salivae (Sal) that will be studied are: a - unstimulated and stimulated (paraffin-activated) salivary flow rates, pH and buffering power; b - quantitative proteomics (QP), on selected targets, representing the main metabolites/components of OM. By matching Sal characteristics with OM and comparing them with OD, it is expected to elucidate their mutual relationship; furthermore, by using specific bioinformatic tools to analyse the data, the potentials of Car in preventing/treating OD and its mechanism of action will be addressed by using QP. The study will take place at the Odontoiatric University Clinic (OUC), Istituto Stomatologico Italiano (ISI) of Milan, Italy, in a prospective, randomised, double-blind, placebo-controlled fashion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oral Diseases
Keywords
dental erosions, caries, périodontopathies

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Controls subjects placebo
Arm Type
Placebo Comparator
Arm Description
Placebo mucoadhesive oral tablet
Arm Title
Controls subjects active Treatment
Arm Type
Experimental
Arm Description
AqualiefTM 400 mg mucoadhesive oral tablet
Arm Title
Diseased subjects placebo
Arm Type
Placebo Comparator
Arm Description
Placebo mucoadhesive oral tablet
Arm Title
Diseased subjects active Treatment
Arm Type
Experimental
Arm Description
AqualiefTM 400 mg mucoadhesive oral tablet
Intervention Type
Dietary Supplement
Intervention Name(s)
400 mg mucoadhesive oral tablet
Intervention Description
AqualiefTM (Metis Healthcare s.r.l., Milano, Italy)
Intervention Type
Dietary Supplement
Intervention Name(s)
placebo mucoadhesive oral tablet
Intervention Description
placebo
Primary Outcome Measure Information:
Title
Effects on oral pH.
Description
Any change of oral pH from basal.
Time Frame
7 days
Title
Saliva Production unstimulated.
Description
Change of oral saliva production, unstimulated.
Time Frame
7 days
Title
Saliva Production stimulated.
Description
Change of oral saliva production, stimulated.
Time Frame
7 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria for Oral Diseased subjects: dental erosions (De) caries (Ca) périodontopathies (Pe) Exclusion Criteria for both: allergies/intolerances to the consumption of Carnosine taking other food supplements any type of drug treatment (interview) smoking pregnancy/lactation any systemic diseases such as cardiovascular and respiratory, diabetes mellitus, HIV infection, or inflammatory conditions causing non-plaque dependent OD.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dino Re, MD
Phone
+39-0254176231
Email
dino.re@unimi.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michele Ciulla, MD
Organizational Affiliation
Lab. Clin. Informatics & Cardiovascular Imaging, University of Milan
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Biomedical, Surgical, and Dental Sciences, Istituto Stomatologico Italiano, Aesthetic Dentistry, School of Dentistry, University of Milan, Milan, Italy.
City
Milan
ZIP/Postal Code
20122
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dino Re

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
18335122
Citation
de Almeida Pdel V, Gregio AM, Machado MA, de Lima AA, Azevedo LR. Saliva composition and functions: a comprehensive review. J Contemp Dent Pract. 2008 Mar 1;9(3):72-80.
Results Reference
result
PubMed Identifier
26662484
Citation
Marsh PD, Do T, Beighton D, Devine DA. Influence of saliva on the oral microbiota. Periodontol 2000. 2016 Feb;70(1):80-92. doi: 10.1111/prd.12098.
Results Reference
result
PubMed Identifier
27102203
Citation
Grassl N, Kulak NA, Pichler G, Geyer PE, Jung J, Schubert S, Sinitcyn P, Cox J, Mann M. Ultra-deep and quantitative saliva proteome reveals dynamics of the oral microbiome. Genome Med. 2016 Apr 21;8(1):44. doi: 10.1186/s13073-016-0293-0.
Results Reference
result
PubMed Identifier
30338752
Citation
Abranches J, Zeng L, Kajfasz JK, Palmer SR, Chakraborty B, Wen ZT, Richards VP, Brady LJ, Lemos JA. Biology of Oral Streptococci. Microbiol Spectr. 2018 Oct;6(5):10.1128/microbiolspec.GPP3-0042-2018. doi: 10.1128/microbiolspec.GPP3-0042-2018.
Results Reference
result
PubMed Identifier
31029715
Citation
Dolan E, Saunders B, Harris RC, Bicudo JEPW, Bishop DJ, Sale C, Gualano B. Comparative physiology investigations support a role for histidine-containing dipeptides in intracellular acid-base regulation of skeletal muscle. Comp Biochem Physiol A Mol Integr Physiol. 2019 Aug;234:77-86. doi: 10.1016/j.cbpa.2019.04.017. Epub 2019 Apr 25.
Results Reference
result
PubMed Identifier
24137022
Citation
Boldyrev AA, Aldini G, Derave W. Physiology and pathophysiology of carnosine. Physiol Rev. 2013 Oct;93(4):1803-45. doi: 10.1152/physrev.00039.2012.
Results Reference
result
PubMed Identifier
22044034
Citation
Ciulla MM, Paliotti R, Carini M, Magrini F, Aldini G. Fibrosis, Enzymatic and Non-Enzymatic Cross-Links in Hypertensive Heart Disease. Cardiovasc Hematol Disord Drug Targets. 2011;11(2):61-73. doi: 10.2174/187152911798347025.
Results Reference
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PubMed Identifier
29567852
Citation
Menon K, Mousa A, de Courten B. Effects of supplementation with carnosine and other histidine-containing dipeptides on chronic disease risk factors and outcomes: protocol for a systematic review of randomised controlled trials. BMJ Open. 2018 Mar 22;8(3):e020623. doi: 10.1136/bmjopen-2017-020623.
Results Reference
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PubMed Identifier
29710488
Citation
Zhang Y, Wang X, Li H, Ni C, Du Z, Yan F. Human oral microbiota and its modulation for oral health. Biomed Pharmacother. 2018 Mar;99:883-893. doi: 10.1016/j.biopha.2018.01.146. Epub 2018 Feb 20.
Results Reference
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PubMed Identifier
25808877
Citation
Holtfreter B, Albandar JM, Dietrich T, Dye BA, Eaton KA, Eke PI, Papapanou PN, Kocher T; Joint EU/USA Periodontal Epidemiology Working Group. Standards for reporting chronic periodontitis prevalence and severity in epidemiologic studies: Proposed standards from the Joint EU/USA Periodontal Epidemiology Working Group. J Clin Periodontol. 2015 May;42(5):407-12. doi: 10.1111/jcpe.12392. Epub 2015 May 7.
Results Reference
result

Learn more about this trial

Carnosine Supplementation on Quantity/Quality of Oral Salivae.

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