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NCT03422692 · ClinicalTrials.gov registry record · Phase 1

Socket Preservation: A Clinical and Histological Study

A Phase 1 study, sponsored by University of Kentucky.

Completed
Registry status
Phase 1
Development phase
43
Enrollment target

NCT03422692: Completed Phase 1 study, sponsored by University of Kentucky.

NCT03422692 is a Phase 1 study that has completed, run by University of Kentucky. The registered enrollment target is 43 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (28% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03422692, a Phase 1 study, has completed, sponsored by University of Kentucky.

COMPLETED
Registry status
Phase 1
Development phase
43 participants
Enrollment target

Study Summary

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.

Primary Outcome

Mean vital bone formation using histomorphometric analysis

Interventions

  • BIOLOGICAL BioXclude amnion-chorion membrane
  • BIOLOGICAL Mem-Lok collagenous membrane

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2013-10-01
Est. Completion 2015-10-01
Phase Phase 1
University of Kentucky

54 total trials

What the finished NCT03422692 record still lists

NCT03422692 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 43 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (28% lower).

The record links to 0 conditions, and to 2 interventions - of which BioXclude amnion-chorion membrane is the first listed.

NCT03422692 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03422692 about?

NCT03422692 is a clinical study titled "Socket Preservation: A Clinical and Histological Study". 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 rand...

What is the current status of trial NCT03422692?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 43 participants. The study started on 2013-10-01. Estimated completion is 2015-10-01.

What interventions are being tested in trial NCT03422692?

The interventions under investigation include: BioXclude amnion-chorion membrane (BIOLOGICAL), Mem-Lok collagenous membrane (BIOLOGICAL).

Who is sponsoring clinical trial NCT03422692?

This trial is sponsored by University of Kentucky, which has 54 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03422692's enrollment target sits among peer trials

43 1100th of 2000 higher than 896 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03422692, the US trial registry maintained by the National Library of Medicine. NCT03422692 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.