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Clinical Trials/NCT05419102
NCT05419102
Completed
N/A

Retrospective Study of Implants With Peri-implantitis Surgically Treated Using Enamel Matrix Derivative (EMD)

North Dallas Dental Health1 site in 1 country34 target enrollmentApril 1, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Determination of Beneficial Effect of Using Enamel Matrix Derivative During Implant Treatment
Sponsor
North Dallas Dental Health
Enrollment
34
Locations
1
Primary Endpoint
retention of the implant
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The existing records of a private practice limited to the practice of periodontology were reviewed to locate patients who had been diagnosed with peri-implantitis (failing dental implant) and had been surgically treated utilizing enamel matrix derivative (Commercially available FDA product Emdogain sold by Straumann USA). Various clinical factors were gathered from the existing records. Some of the factors recorded were: retention of the implant, presence of bleeding, presence of further damage, and presence of inflammation. All patients had signed an informed consent for treatment and the anonymous use of their data for research purposes. All HIPA requirements were followed.

Detailed Description

See brief summary.

Registry
clinicaltrials.gov
Start Date
April 1, 2022
End Date
June 6, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Thomas G Wilson, Jr. DDS

Private Practitioner

North Dallas Dental Health

Eligibility Criteria

Inclusion Criteria

  • all adult patients of record who presented with existing peri-implantitis that was clinically deemed treatable (the implant was not considered hopeless.)

Exclusion Criteria

  • none except for routine medical contraindications for periodontal surgery

Outcomes

Primary Outcomes

retention of the implant

Time Frame: 0.71 to 6.4 years

Determine if the implant was still present at the time of reevaluation

Secondary Outcomes

  • record the clinical condition of the implant at the time of reevaluation(0.71 to 6.4 years)

Study Sites (1)

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