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Locally Delivered Minocycline in Advanced Periodontitis

Primary Purpose

Periodontitis, Adult

Status
Completed
Phase
Phase 4
Locations
Malaysia
Study Type
Interventional
Intervention
Minocycline Hydrochloride
Sponsored by
Mahsa University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Periodontitis, Adult

Eligibility Criteria

25 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • systematically healthy patients with age range between 20- 60 years,
  • diagnosed with untreated Advanced Periodontitis with a pocket depth ≥6mm around two or more teeth, in two or more quadrants.

Exclusion Criteria:

  • Patients given antibiotics or anti-inflammatory drugs in the past 6 months,
  • allergic to tetracycline,
  • pregnant or nursing females,
  • those using chlorhexidine or any other mouth rinse

Sites / Locations

  • MAHSA University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Minocycline

Placebo

Arm Description

Minocycline gel

Similar gel without the active agent

Outcomes

Primary Outcome Measures

Change in Probing pocket depth (PPD)
Periodontal pocket is measured from the gingival margin to the base of the periodontal pocket using a UNC periodontal probe (which is graduated from 1mm to 15mm). The measurement of periodontal pocket depth is a continuous scale. PPD is taken at 6 points on each tooth. The mean of the PPD will be obtained for each patient and subjected to statistical analysis.
Change in the numbers of Periodontal pathogens
Plaque samples taken from periodontal pockets on paper points will be first stored and later analysed for the presence and number of periopathogens using quantative Polymerase Chain Reaction (q-PCR). The following periodontal pathogens will be assessed: Red complex (Porphyromonas gingivalis, Tannerella forsythia,and Treponema denticola) Filifactor alocis, oral phylotypes of phyla Synergistetes Phylum TM7
Clinical Attachment Levels (CAL)
change in CAL

Secondary Outcome Measures

Plaque Index
change in Plaque scores (Silness and Loe Plaque index, 1964) The score ranges from 0-3 and it is a continuous scale. '0' - no plaque '1' - thin plaque which is not visible by naked eye '2' - Moderate accumulation plaque seen by naked eye '3' - abundance of plaque. Calculation total score /number of surfaces examined = Index score for each patient. Mean plaque score is calculated for all the patients.
Bleeding Index
change in Bleeding scores (Papillary bleeding index, Muehlemann 1977) The score ranges from 0-4 and it is a continuous scale. '0' - no bleeding '1' - Single discrete bleeding point '2' - Single line of blood appears '3' - Interdental papilla fills with blood after probing '4' - profuse bleeding after probing Calculation total score /number of surfaces examined = Index score for each patient. Mean plaque score is calculated for all the patients.

Full Information

First Posted
August 2, 2019
Last Updated
September 21, 2021
Sponsor
Mahsa University
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1. Study Identification

Unique Protocol Identification Number
NCT04076098
Brief Title
Locally Delivered Minocycline in Advanced Periodontitis
Official Title
Efficacy of Locally Delivered Minocycline in Advanced Periodontitis. A Clinico-microbiological Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
June 25, 2018 (Actual)
Primary Completion Date
December 28, 2020 (Actual)
Study Completion Date
September 20, 2021 (Actual)

3. Sponsor/Collaborators

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

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
Local drug delivery provides higher concentrations in the availability of the drug at the specific infected sites with the advantage of sustained release. Periocline is a long acting , sustained release local drug delivery system consisting of 2% minocycline hydrochloride in an ointment containing microcapsule type particles. Periocline contains 20mg of minocycline in 0.5 gm of gel in a disposable polypropylene applicator (2% minocycline HCl). Research has yielded promising results with the local application of minocycline in the treatment of periodontal disease, compared with other non-surgical therapies. However, there is scarcity of reports on the use of local delivery agents with respect to new range of putative pathogens in advanced periodontitis, wherein the tissue invasive anaerobic organisms are present and possibly compromised host response, hence resulting in an exaggerated breakdown of periodontal tissues at the affected sites. The effect of Minocycline on new putative pathogens, such as Filifactor alocis and oral phylotypes of phyla Synergistetes and TM7 (referred to hereafter as oral Synergistetes and oral TM7s), has not been investigated yet. Hence, the aim of the present study is to evaluate the efficacy of a local delivery agent containing minocycline (Periocline, Sunstar, Japan) as an adjunct to SRP in the treatment of deep periodontal pockets around teeth in advanced periodontitis and the antimicrobial effect on the red complex and the new putative pathogens.
Detailed Description
The subjects for this randomized controlled, parallel arm study will be selected from the primary health care in the Faculty of Dentistry, MAHSA University. In this clinical trial, 50 patients with advanced periodontitis will be enrolled in the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Periodontitis, Adult

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Minocycline
Arm Type
Experimental
Arm Description
Minocycline gel
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Similar gel without the active agent
Intervention Type
Drug
Intervention Name(s)
Minocycline Hydrochloride
Other Intervention Name(s)
Periocline
Intervention Description
Administration of Periocline gel into the periodontal pockets will be carried out until it overflows the pockets
Primary Outcome Measure Information:
Title
Change in Probing pocket depth (PPD)
Description
Periodontal pocket is measured from the gingival margin to the base of the periodontal pocket using a UNC periodontal probe (which is graduated from 1mm to 15mm). The measurement of periodontal pocket depth is a continuous scale. PPD is taken at 6 points on each tooth. The mean of the PPD will be obtained for each patient and subjected to statistical analysis.
Time Frame
baseline to 12 weeks
Title
Change in the numbers of Periodontal pathogens
Description
Plaque samples taken from periodontal pockets on paper points will be first stored and later analysed for the presence and number of periopathogens using quantative Polymerase Chain Reaction (q-PCR). The following periodontal pathogens will be assessed: Red complex (Porphyromonas gingivalis, Tannerella forsythia,and Treponema denticola) Filifactor alocis, oral phylotypes of phyla Synergistetes Phylum TM7
Time Frame
baseline to 12 weeks
Title
Clinical Attachment Levels (CAL)
Description
change in CAL
Time Frame
baseline, 6 weeks and 12 weeks
Secondary Outcome Measure Information:
Title
Plaque Index
Description
change in Plaque scores (Silness and Loe Plaque index, 1964) The score ranges from 0-3 and it is a continuous scale. '0' - no plaque '1' - thin plaque which is not visible by naked eye '2' - Moderate accumulation plaque seen by naked eye '3' - abundance of plaque. Calculation total score /number of surfaces examined = Index score for each patient. Mean plaque score is calculated for all the patients.
Time Frame
baseline to 12 weeks
Title
Bleeding Index
Description
change in Bleeding scores (Papillary bleeding index, Muehlemann 1977) The score ranges from 0-4 and it is a continuous scale. '0' - no bleeding '1' - Single discrete bleeding point '2' - Single line of blood appears '3' - Interdental papilla fills with blood after probing '4' - profuse bleeding after probing Calculation total score /number of surfaces examined = Index score for each patient. Mean plaque score is calculated for all the patients.
Time Frame
baseline to 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: systematically healthy patients with age range between 20- 60 years, diagnosed with untreated Advanced Periodontitis with a pocket depth ≥6mm around two or more teeth, in two or more quadrants. Exclusion Criteria: Patients given antibiotics or anti-inflammatory drugs in the past 6 months, allergic to tetracycline, pregnant or nursing females, those using chlorhexidine or any other mouth rinse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tara Taiyeb Ali, MSc, FDSRCS
Organizational Affiliation
Mahsa University
Official's Role
Principal Investigator
Facility Information:
Facility Name
MAHSA University
City
Jenjarum
State/Province
Selangor
ZIP/Postal Code
42610
Country
Malaysia

12. IPD Sharing Statement

Plan to Share IPD
No

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Locally Delivered Minocycline in Advanced Periodontitis

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