Socket Preservation: A Clinical and Histological Study

Completed · Phase 1

Conditions studied: Alveolar Ridge Augmentations

In brief

The objective of this study is to investigate the use of human amnion chorion membrane (BioXclude®) as an exposed barrier in ridge preservation and whether the intentional exposure of this membrane to oral environment will adversely affect ridge healing, dimensions, and bone vitality. This is a randomized clinical study.

Key facts

Study ID

NCT03422692

Run by

University of Kentucky

People needed

43

Starts

2013-10-01

Expected to finish

2015-10-01

Last updated by the study team

2018-02-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• must have an unsalvageable tooth with extraction planned with delayed implant
• extraction sockets must have intact buccal and lingual cortical plates

You may not qualify if…

• completely endentulous
• plan for a full mouth tooth extraction
• radiation therapy
• uncontrolled systemic disorders
• acute odontogenic infections
• smoking >10 cigarettes/day
• taking anti-resorptive meds
• pregnant or may become pregnant

Where it is running

• University of Kentucky College of Dentistry — Lexington, Kentucky, United States

Full record on ClinicalTrials.gov

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