ClinicalTrials.Veeva

Menu

Effect of Enamel Matrix Proteins on Clinical Attachment Level and Alveolar Bone in Periodontal Maintenance Patients

University of Nebraska logo

University of Nebraska

Status and phase

Completed
Early Phase 1

Conditions

Periodontal Bone Loss

Treatments

Other: Saline
Drug: Enamel Matrix Proteins Derivative

Study type

Interventional

Funder types

Other

Identifiers

NCT02972788
0783-16-FB

Details and patient eligibility

About

The purpose of the study is to determine the effect of enamel matrix protein derivative on an inflamed, periodontal-involved tooth. The hypothesis to be studied is that enamel matrix derivative protein with increase the clinical attachment level is localized sites of advanced periodontal disease.

Full description

The purpose of this study is to determine if local application of a commercially-available, FDA-approved preparation of enamel-matrix protein derivatives is effective in increasing clinical attachment levels (primary outcome), as well as alveolar bone (secondary outcome) compared to standard mechanical therapy in patients on periodontal maintenance therapy (PMT). Subjects will be divided into two groups for additional therapy in a 6-9 mm interproximal periodontal pocket at baseline: 1) local anesthesia and mini-flap reflection with subgingival mechanical debridement plus application of the enamel matrix protein derivate or 2) local anesthesia and mini-flap reflection with subgingival mechanical debridement plus application of saline. Samples/measurements will be obtained at the designated experimental site at baseline, 2 weeks, 6 and 12 months during PMT: 1) digital radiograph (baseline and 12 months only; bone height measurements), 2) presence of explorer-detectable supragingival plaque, 3) 30-second gingival crevicular fluid (GCF) sample (markers of inflammation, bone turnover), 4) recession from the cemento-enamel junction, 5) probing pocket depth and bleeding on probing (BOP). Following the 12-month visit, the research-specific interventions and measurements in the experimental quadrant will be removed from routine PMT.

Enrollment

50 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosis of chronic advanced adult periodontitis
  • one quadrant with at least one 6-9 mm interproximal pocket
  • overall good systemic health
  • willingness to sign consent form

Exclusion criteria

  • systemic diseases which significantly impact periodontal inflammation and bone turnover (e.g. rheumatoid arthritis)
  • taking drugs which significantly impact periodontal inflammation and bone turnover
  • surgical periodontal therapy within the past year
  • pregnant or breast-feeding females

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 2 patient groups

Experimental Group
Experimental group
Description:
Group will receive enamel matrix protein derivative treatment along with scaling and root planing.
Treatment:
Drug: Enamel Matrix Proteins Derivative
Control Group
Sham Comparator group
Description:
Group will receive placebo (saline) treatment along with scaling and root planing.
Treatment:
Other: Saline

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems