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Enamel Matrix Derivative in Non-surgical Periodontal Treatment

Primary Purpose

Periodontitis

Status
Completed
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
Emdogain® FL
Scaling and root planing
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Periodontitis focused on measuring Enamel Matrix Derivative, Periodontitis, Non-surgical periodontal therapy

Eligibility Criteria

25 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Periodontitis stage III
  • Patients that have completed initial periodontal therapy, and have remaining periodontal pockets of ≥6mm up to 9mm PPD
  • Given written informed consent form for participation in the study

Exclusion Criteria:

  • Systemic antibiotics within the previous 3 months
  • Pregnant or breastfeeding women
  • Any current or past clinically significant pathology/disease (comorbidity) that, in the opinion of the periodontists, might confound the results or poses an additional risk to the subject during participation in the study, such as renal insufficiency, malignancy, rheumatoid osteoarthritis, human immunodeficiency syndrome.
  • Patients with at least one tooth of mobility grade 0 or 1 and/or furcation involvement grade 0 or I according to Hamp

Sites / Locations

  • University Clinic of Dentistry Vienna

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Emdogain® FL

Control group

Arm Description

Non-surgical periodontal therapy in terms of scaling and root planing will be applied at sites with remaining periodontal pockets at reevaluation. EDTA gel will be applied for 2 minutes in the respective pockets, followed by rinsing with saline, drying and application of Emdogain® FL.

Non-surgical periodontal therapy in terms of scaling and root planing will be applied at sites with remaining periodontal pockets at reevaluation, followed by rinsing with saline.

Outcomes

Primary Outcome Measures

Periodontal probing depth (PPD)
Distance from the gingival margin to the base of the pocket with a calibrated periodontal probe
Periodontal probing depth (PPD)
Distance from the gingival margin to the base of the pocket with a calibrated periodontal probe
Periodontal probing depth (PPD)
Distance from the gingival margin to the base of the pocket with a calibrated periodontal probe
Periodontal probing depth (PPD)
Distance from the gingival margin to the base of the pocket with a calibrated periodontal probe

Secondary Outcome Measures

CAL (mm)
CAL (Clinical attachment level): the probing depth and the distance from the gingival margin to the CEJ API: Approximal plaque index PBI: Papillary Bleeding Index PESA:Periodontal Epithelial Surface Area PISA: periodontal inflamed surface area GCF: Gingival crevicular fluid
API, PBI (%)
API: Approximal plaque index PBI: Papillary Bleeding Index
PESA, PISA (mm2)
PESA:Periodontal Epithelial Surface Area PISA: periodontal inflamed surface area
GCF markers for periodontal regeneration
GCF: Gingival crevicular fluid
Periodontal bacteria
Microbiologic evaluation of GCF via polymerase chain reaction (PCR) DNA probe test kit

Full Information

First Posted
June 20, 2020
Last Updated
October 22, 2022
Sponsor
Medical University of Vienna
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1. Study Identification

Unique Protocol Identification Number
NCT04449393
Brief Title
Enamel Matrix Derivative in Non-surgical Periodontal Treatment
Official Title
Effect of Enamel Matrix Derivative in the Non-surgical Treatment of Periodontal Maintenance Patients
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
September 15, 2020 (Actual)
Primary Completion Date
May 1, 2022 (Actual)
Study Completion Date
July 1, 2022 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the study is to investigate the effect of enamel matrix derivative in addition to scaling and root planing in comparison to scaling and root planing only in periodontitis patients that have already undergone initial periodontal therapy and are in periodontal maintenance.
Detailed Description
Enamel matrix derivative (EMD) have already been widely applied as a regenerative bio-modulator in periodontal surgery and have been demonstrated to enhance periodontal regeneration. Recently, also its flapless, non-surgical application has been shown to have beneficial effects when applied during initial therapy of periodontitis. The present study is designed as a single-blinded randomized controlled clinical trial. We plan to include a total of 50 periodontitis patients that have already undergone initial periodontal therapy, but still show remaining sites with increased periodontal probing depth (PPD). Patients will be randomly allocated at a 1:1 ratio to either scaling and root planing (SRP) in combination with EMD application into the affected pockets (test group, n=25) or to SRP only (control group, n=25). Before treatment, as well as after 3, 6 and 12 months, we plan to assess site-specific periodontal parameters as well as whole-mouth oral hygiene indices. Furthermore, we intend to evaluate gingival crevicular fluid, as well as parameters representing periodontal disease activity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Periodontitis
Keywords
Enamel Matrix Derivative, Periodontitis, Non-surgical periodontal therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Emdogain® FL
Arm Type
Experimental
Arm Description
Non-surgical periodontal therapy in terms of scaling and root planing will be applied at sites with remaining periodontal pockets at reevaluation. EDTA gel will be applied for 2 minutes in the respective pockets, followed by rinsing with saline, drying and application of Emdogain® FL.
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Non-surgical periodontal therapy in terms of scaling and root planing will be applied at sites with remaining periodontal pockets at reevaluation, followed by rinsing with saline.
Intervention Type
Device
Intervention Name(s)
Emdogain® FL
Intervention Description
Emdogain® FL is an enamel matrix derivative intended for subgingival and topical application in conjunction with scaling and root planing procedures to provide regeneration of tooth support lost due to periodontal disease. Emdogain® FL has been shown to be effective in residual pockets with probing depths from 5mm to 9mm with no furcation involvement in patients with adequate plaque control. Emdogain® FL has also been shown to enhance the early healing of periodontal soft tissue wounds resulting from the instrumentation of periodontal pockets.
Intervention Type
Other
Intervention Name(s)
Scaling and root planing
Intervention Description
Scaling and root planing procedures as part of non-surgical periodontal therapy involves mechanical removal of dental plaque and calculus using curettes and sonic scalers.
Primary Outcome Measure Information:
Title
Periodontal probing depth (PPD)
Description
Distance from the gingival margin to the base of the pocket with a calibrated periodontal probe
Time Frame
At baseline
Title
Periodontal probing depth (PPD)
Description
Distance from the gingival margin to the base of the pocket with a calibrated periodontal probe
Time Frame
After 3 months
Title
Periodontal probing depth (PPD)
Description
Distance from the gingival margin to the base of the pocket with a calibrated periodontal probe
Time Frame
After 6 months
Title
Periodontal probing depth (PPD)
Description
Distance from the gingival margin to the base of the pocket with a calibrated periodontal probe
Time Frame
After 12 months
Secondary Outcome Measure Information:
Title
CAL (mm)
Description
CAL (Clinical attachment level): the probing depth and the distance from the gingival margin to the CEJ API: Approximal plaque index PBI: Papillary Bleeding Index PESA:Periodontal Epithelial Surface Area PISA: periodontal inflamed surface area GCF: Gingival crevicular fluid
Time Frame
At baseline, after 3, 6 and 12 months
Title
API, PBI (%)
Description
API: Approximal plaque index PBI: Papillary Bleeding Index
Time Frame
At baseline, after 3, 6 and 12 months
Title
PESA, PISA (mm2)
Description
PESA:Periodontal Epithelial Surface Area PISA: periodontal inflamed surface area
Time Frame
At baseline, after 3, 6 and 12 months
Title
GCF markers for periodontal regeneration
Description
GCF: Gingival crevicular fluid
Time Frame
At baseline, after 3, 6 and 12 months
Title
Periodontal bacteria
Description
Microbiologic evaluation of GCF via polymerase chain reaction (PCR) DNA probe test kit
Time Frame
At baseline, after 3, 6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Periodontitis stage III Patients that have completed initial periodontal therapy, and have remaining periodontal pockets of ≥6mm up to 9mm PPD Given written informed consent form for participation in the study Exclusion Criteria: Systemic antibiotics within the previous 3 months Pregnant or breastfeeding women Any current or past clinically significant pathology/disease (comorbidity) that, in the opinion of the periodontists, might confound the results or poses an additional risk to the subject during participation in the study, such as renal insufficiency, malignancy, rheumatoid osteoarthritis, human immunodeficiency syndrome. Patients with at least one tooth of mobility grade 0 or 1 and/or furcation involvement grade 0 or I according to Hamp
Facility Information:
Facility Name
University Clinic of Dentistry Vienna
City
Vienna
ZIP/Postal Code
1090
Country
Austria

12. IPD Sharing Statement

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Enamel Matrix Derivative in Non-surgical Periodontal Treatment

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