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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03392038
Other study ID # 16.0462
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 30, 2017
Est. completion date August 21, 2018

Study information

Verified date September 2020
Source University of Louisville
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To study and compare a thick vs thin acellular dermal matrix for root coverage using the coronally positioned tunnel technique.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date August 21, 2018
Est. primary completion date August 21, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

A. At least one Miller Class I or II mucogingival defect = 3 mm (Miller 1985). B. The mucogingival defect must be on a non-molar tooth. C. Patients must be = 18 years of age.

Exclusion Criteria:

A. Patients with debilitating systemic or diseases that significantly affect the periodontium.

B. Patients with a known allergy to any of the materials that will be used in the study, including systemic antibiotics (tetracycline and doxycycline).

C. Patients requiring antibiotic prophylaxis. D. Root surface restorations at the site of recession. E. No detectable CEJ F. Patients who fail to maintain acceptable oral hygiene levels at the test and adjacent teeth.

G. Patients who are pregnant or lactating. H. Patients who use tobacco products (smoking or smokeless tobacco). I. Patients with alcohol abuse problems. J. Patients undergoing long-term steroid therapy. K. History of previous root coverage procedures, graft or GTR, on the test teeth.

L. Patients who fail to complete the informed consent form.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Thin ADM
Use of soft tissue allograft for root coverage
Thick ADM
Periodontal surgical procedure to coronally position the tissue over the ADM allograft

Locations

Country Name City State
United States Graduate Periodontics, UofL School of Dentistry Louisville Kentucky

Sponsors (1)

Lead Sponsor Collaborator
University of Louisville

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percent root coverage Between 0 and 100% Six months
Secondary Creeping Attachment Amount in millimeters Six months
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