Trials Sponsors Conditions Drugs Pricing

Conditions

Alveolar Ridge Augmentations

Keywords

Resorbable membrane, amnion-chorion membrane, collagen membrane, ridge preservation.

Outcome Measures

Primary Outcomes (1)

bone quality
Mean vital bone formation using histomorphometric analysis
19.5 weeks post intervention

Secondary Outcomes (1)

Bone quantity
19.5 weeks post intervention

Study Arms (2)

BioXlude memebrane

EXPERIMENTAL

Subjects in this arm will receive demineralized freeze dried bone allograft covered with BioXclude amnion-chorion membrane following tooth extraction

Biological: BioXclude amnion-chorion membrane

Mem-Lok

ACTIVE COMPARATOR

subjects in this arm will receive demineralized freeze dried bone allograft covered with Mem-Lok collagenous membrane following tooth extraction

Biological: Mem-Lok collagenous membrane

Interventions

BioXclude amnion-chorion membraneBiological

BioXclude will be used for the prevention of alveolar ridge resorption via socket bone graft and amnion-chorion membrane closure

Also known as: BioXclude membrane

BioXlude memebrane

Mem-Lok collagenous membraneBiological

Mem-Lok will be used for the prevention of alveolar ridge resorption via socket bone graft and collagenous membrane closure

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

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:

Sponsors & Collaborators

University of Kentucky
Otherlead

Study Sites (1)

University of Kentucky College of Dentistry

Lexington, Kentucky, 40536, United States

Study Officials

Mohanad Al-Sabbagh, DDS, MS
University of Kentucky
PRINCIPAL INVESTIGATOR

Enrollment

43 participants (actual enrollment reported by the registry).

Study Design

Study Type: interventional
Phase: phase 1
Allocation: RANDOMIZED
Masking: SINGLE
Who Masked: PARTICIPANT
Purpose: TREATMENT
Intervention Model: PARALLEL
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Professor and Chief of Periodontology

Study Record Dates

First Submitted

January 30, 2018

First Posted

February 6, 2018

Study Start

October 1, 2013

Actual (reported)

Socket Preservation: A Clinical and Histological Study

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (2)

BioXlude memebrane

Mem-Lok

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Enrollment

Study Design

Study Record Dates

Data Sharing

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (2)

BioXlude memebrane

Mem-Lok

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Enrollment

Study Design

Study Record Dates

Data Sharing

Source record

Locations