Skip to content

Enamel Matrix Derivative in Non-surgical Periodontal Treatment

Effect of Enamel Matrix Derivative in the Non-surgical Treatment of Periodontal Maintenance Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04449393
Enrollment
22
Registered
2020-06-26
Start date
2020-09-15
Completion date
2022-07-01
Last updated
2022-10-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Periodontitis

Keywords

Enamel Matrix Derivative, Periodontitis, Non-surgical periodontal therapy

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.

Interventions

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.

OTHERScaling and root planing

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.

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
25 Years to 75 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Periodontal probing depth (PPD)At baselineDistance from the gingival margin to the base of the pocket with a calibrated periodontal probe

Secondary

MeasureTime frameDescription
PESA, PISA (mm2)At baseline, after 3, 6 and 12 monthsPESA:Periodontal Epithelial Surface Area PISA: periodontal inflamed surface area
GCF markers for periodontal regenerationAt baseline, after 3, 6 and 12 monthsGCF: Gingival crevicular fluid
Periodontal bacteriaAt baseline, after 3, 6 and 12 monthsMicrobiologic evaluation of GCF via polymerase chain reaction (PCR) DNA probe test kit
CAL (mm)At baseline, after 3, 6 and 12 monthsCAL (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 (%)At baseline, after 3, 6 and 12 monthsAPI: Approximal plaque index PBI: Papillary Bleeding Index

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026