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New Periodontitis Treatment Based on Hyaluronic Acid and Melatonin (HAMELDENT)

Primary Purpose

Chronic Periodontitis

Status
Completed
Phase
Phase 2
Locations
Romania
Study Type
Interventional
Intervention
Tetracycline-Metronidazole (TM) group
TM-Melatonin-Hyaluronic acid (TM-MHa) group
Sponsored by
Concordia Dent Srl
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Periodontitis focused on measuring Melatonin, Hyaluronic Acid, Tetracycline, Metronidazole, topic paste, chronic periodontitis

Eligibility Criteria

30 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • moderate chronic periodontitis, that is, > 2 interproximal sites with AL > 4 mm (not on the same tooth), or > 2 interproximal sites with pocket depth (PD) > 5 mm (not on the same tooth) (1),
  • at least 20 teeth present in the mouth,
  • no periodontal therapy during the last 6 months,
  • no antibiotic during the last 6 months,
  • good general health (no systemic condition affecting the course of periodontal disease, including malignancy), pregnancy,
  • no allergy to the product components,
  • good mental health.

Exclusion Criteria:

  • Patients not willing to sign consent form.
  • Patients not agreeing with the treatment protocol.

Sites / Locations

  • Concordia Dent Clinic
  • "Carol Davila"University of Medicine and Pharmacy

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Tetracycline-Metronidazole (TM) group

TM-Melatonin-Hyaluronic acid (TM-MHa) group

Arm Description

Topical administration (in the periodontal pocket of affected teeth), for 30 consecutive days of 3%Tetracycline and 3%Metronidazole paste (TM), n=25 patients, considered control group.

Topical administration (in the periodontal pocket of affected teeth), for 30 consecutive days of 3% Tetracycline, 3% Metronidazole, 0.18% Melatonin and 3% Hyaluronic Acid (TM-MHa) paste, n=25 patients, considered experimental group.

Outcomes

Primary Outcome Measures

Changes in Clinical attachment level (CAL)
Changes CAL from Baseline (before treatment) at 6 months will be assessed using a standardised protocol.

Secondary Outcome Measures

Changes in Alveolar bone height
Changes in the alveolar bone height from Baseline (before treatment) at 6 months will be assessed using standardised Radiographic measurements.
Treatment's influence on bactrial pathogens
Periodontal pathogens will be identified by performing micro-IDent® assay before treatment (Baseline) and 6 month after its completion. Micro-IDent® test uses chain polymerisation reaction, with colorimetric detection, to identify the following pathogens: Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, Bacteroides forsythus, Treponema denticola.

Full Information

First Posted
August 29, 2018
Last Updated
January 23, 2020
Sponsor
Concordia Dent Srl
Collaborators
Carol Davila University of Medicine and Pharmacy, Romanian National Authority for Scientific Research and Innovation (UEFISCIDI), University Politechnica of Bucharest, TURKEY MEDISEN Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT03656484
Brief Title
New Periodontitis Treatment Based on Hyaluronic Acid and Melatonin
Acronym
HAMELDENT
Official Title
Innovative Technology for Assessing the Periodontal Disease and New Periodontitis Treatment Based on Hyaluronic Acid and Melatonin
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
January 15, 2019 (Actual)
Primary Completion Date
December 20, 2019 (Actual)
Study Completion Date
December 20, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Concordia Dent Srl
Collaborators
Carol Davila University of Medicine and Pharmacy, Romanian National Authority for Scientific Research and Innovation (UEFISCIDI), University Politechnica of Bucharest, TURKEY MEDISEN Ltd

4. Oversight

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

5. Study Description

Brief Summary
The aim of the present study is to determine whether the association of Melatonin and Hyaluronic Acid to the antimicrobial TM paste (3% Tetracyclin and 3% Metronidazole) for periodontal maintenance therapy can improve the attachment level (AL) and alveolar bone support for moderate chronic periodontitis.
Detailed Description
Local drug delivery agents in periodontology has gained acceptance and popularity compared to systemic drugs due to decreased risk in development of resistant flora, opportunist infection, and side effects. In order to improve the topical treatment for chronic periodontitis, Melatonin and Hyaluronic Acid have been added to antimicrobial topic paste commercially available. A complex matrix composed of Tetracycline, Metronidazole, Melatonin and Hyaluronic Acid have been developed for local treatment of chronic periodontitis. Microbiological, physical, chemical characterization of the newly obtained matrix and biocompatibility tests have been performed. A randomized clinical trial will be perform on 50 patients with moderate chronic periodontitis recruited based on eligibility criteria and informed consent signed. Mechanical debridement of the pockets by scaling and root planning will be performed prior to the adjunctive therapy. Extensive clinical examination including charting the remaining teeth, clinical attachment level (CAL), presence of dental plaque (PI), gingival index (GI), calculus (CI), bleeding on probing (BOP), radiographic assessment and identification of periodontal pathogens with micro-IDent® test will be performed at the beginning of the study and 6 month after its completion. Each patient will be randomized using sealed envelopes (according to a computer-generated randomization list) to one of the following topical administration (in the periodontal pocket of affected teeth), for 30 consecutive days: Tetracycline and Metronidazole paste (TM), n=25 patients and Tetracycline, Metronidazole, Melatonin, Hyaluronic Acid paste (TM-MHa), n=25 patients. A statistical evaluation of data recorded during the entire follow-up period will be performed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Periodontitis
Keywords
Melatonin, Hyaluronic Acid, Tetracycline, Metronidazole, topic paste, chronic periodontitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tetracycline-Metronidazole (TM) group
Arm Type
Active Comparator
Arm Description
Topical administration (in the periodontal pocket of affected teeth), for 30 consecutive days of 3%Tetracycline and 3%Metronidazole paste (TM), n=25 patients, considered control group.
Arm Title
TM-Melatonin-Hyaluronic acid (TM-MHa) group
Arm Type
Experimental
Arm Description
Topical administration (in the periodontal pocket of affected teeth), for 30 consecutive days of 3% Tetracycline, 3% Metronidazole, 0.18% Melatonin and 3% Hyaluronic Acid (TM-MHa) paste, n=25 patients, considered experimental group.
Intervention Type
Drug
Intervention Name(s)
Tetracycline-Metronidazole (TM) group
Other Intervention Name(s)
TM group
Intervention Description
Following mechanical debridement (scaling and root planning) the above-mentioned paste will be topically administrated in the periodontal pocket of affected teeth once a day, for 30 consecutive days.
Intervention Type
Drug
Intervention Name(s)
TM-Melatonin-Hyaluronic acid (TM-MHa) group
Other Intervention Name(s)
TM-MHa group
Intervention Description
Following mechanical debridement (scaling and root planning) the above-mentioned paste will be topically administrated in the periodontal pocket of affected teeth once a day, for 30 consecutive days.
Primary Outcome Measure Information:
Title
Changes in Clinical attachment level (CAL)
Description
Changes CAL from Baseline (before treatment) at 6 months will be assessed using a standardised protocol.
Time Frame
before treatment (Baseline), at 6 months post treatment completion
Secondary Outcome Measure Information:
Title
Changes in Alveolar bone height
Description
Changes in the alveolar bone height from Baseline (before treatment) at 6 months will be assessed using standardised Radiographic measurements.
Time Frame
before treatment (Baseline), at 6 months post treatment completion
Title
Treatment's influence on bactrial pathogens
Description
Periodontal pathogens will be identified by performing micro-IDent® assay before treatment (Baseline) and 6 month after its completion. Micro-IDent® test uses chain polymerisation reaction, with colorimetric detection, to identify the following pathogens: Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, Bacteroides forsythus, Treponema denticola.
Time Frame
before treatment (Baseline), at 6 months post treatment completion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: moderate chronic periodontitis, that is, > 2 interproximal sites with AL > 4 mm (not on the same tooth), or > 2 interproximal sites with pocket depth (PD) > 5 mm (not on the same tooth) (1), at least 20 teeth present in the mouth, no periodontal therapy during the last 6 months, no antibiotic during the last 6 months, good general health (no systemic condition affecting the course of periodontal disease, including malignancy), pregnancy, no allergy to the product components, good mental health. Exclusion Criteria: Patients not willing to sign consent form. Patients not agreeing with the treatment protocol.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
CORINA MARILENA CRISTACHE
Organizational Affiliation
Carol Davila University of Medicine and Pharmacy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Concordia Dent Clinic
City
Bucharest
ZIP/Postal Code
041335
Country
Romania
Facility Name
"Carol Davila"University of Medicine and Pharmacy
City
Bucharest
Country
Romania

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22420873
Citation
Eke PI, Page RC, Wei L, Thornton-Evans G, Genco RJ. Update of the case definitions for population-based surveillance of periodontitis. J Periodontol. 2012 Dec;83(12):1449-54. doi: 10.1902/jop.2012.110664. Epub 2012 Mar 16.
Results Reference
background
PubMed Identifier
25494600
Citation
Feres M, Figueiredo LC, Soares GM, Faveri M. Systemic antibiotics in the treatment of periodontitis. Periodontol 2000. 2015 Feb;67(1):131-86. doi: 10.1111/prd.12075.
Results Reference
background
PubMed Identifier
23320860
Citation
Matesanz-Perez P, Garcia-Gargallo M, Figuero E, Bascones-Martinez A, Sanz M, Herrera D. A systematic review on the effects of local antimicrobials as adjuncts to subgingival debridement, compared with subgingival debridement alone, in the treatment of chronic periodontitis. J Clin Periodontol. 2013 Mar;40(3):227-41. doi: 10.1111/jcpe.12026. Epub 2013 Jan 16.
Results Reference
background
PubMed Identifier
27045432
Citation
Jepsen K, Jepsen S. Antibiotics/antimicrobials: systemic and local administration in the therapy of mild to moderately advanced periodontitis. Periodontol 2000. 2016 Jun;71(1):82-112. doi: 10.1111/prd.12121.
Results Reference
background
PubMed Identifier
12096835
Citation
Koyama H, Nakade O, Takada Y, Kaku T, Lau KH. Melatonin at pharmacologic doses increases bone mass by suppressing resorption through down-regulation of the RANKL-mediated osteoclast formation and activation. J Bone Miner Res. 2002 Jul;17(7):1219-29. doi: 10.1359/jbmr.2002.17.7.1219.
Results Reference
background
PubMed Identifier
29075409
Citation
Montero J, Lopez-Valverde N, Ferrera MJ, Lopez-Valverde A. Changes in crevicular cytokines after application of melatonin in patients with periodontal disease. J Clin Exp Dent. 2017 Sep 1;9(9):e1081-e1087. doi: 10.4317/jced.53934. eCollection 2017 Sep.
Results Reference
background
PubMed Identifier
26692007
Citation
Andersen LP, Gogenur I, Rosenberg J, Reiter RJ. The Safety of Melatonin in Humans. Clin Drug Investig. 2016 Mar;36(3):169-75. doi: 10.1007/s40261-015-0368-5.
Results Reference
background
PubMed Identifier
29438204
Citation
Diker N, Gulsever S, Koroglu T, Yilmaz Akcay E, Oguz Y. Effects of Hyaluronic Acid and Hydroxyapatite/Beta-tricalcium Phosphate in Combination on Bone Regeneration of a Critical-size Defect in an Experimental Model. J Craniofac Surg. 2018 Jun;29(4):1087-1093. doi: 10.1097/SCS.0000000000004338.
Results Reference
background
PubMed Identifier
10328647
Citation
Pirnazar P, Wolinsky L, Nachnani S, Haake S, Pilloni A, Bernard GW. Bacteriostatic effects of hyaluronic acid. J Periodontol. 1999 Apr;70(4):370-4. doi: 10.1902/jop.1999.70.4.370.
Results Reference
background
PubMed Identifier
17325947
Citation
Sakai A, Akifusa S, Itano N, Kimata K, Kawamura T, Koseki T, Takehara T, Nishihara T. Potential role of high molecular weight hyaluronan in the anti-Candida activity of human oral epithelial cells. Med Mycol. 2007 Feb;45(1):73-9. doi: 10.1080/13693780601039607.
Results Reference
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New Periodontitis Treatment Based on Hyaluronic Acid and Melatonin

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