MedTrace Logo

Ridge Preservation Comparing 2 Membranes

NCT01905280 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2016-12-08

No results posted yet for this study

Summary

The purpose of this study is to compare the clinical and histologic outcomes for acellular dermal matrix and a nonresorbable membrane to determine if either provides a significant therapeutic advantage. The hypothesis is that there will be no difference in crestal ridge width between the two treatments.

Conditions

  • Alveolar Ridge Deficiency

Interventions

PROCEDURE

Non-resorbable membrane

The ridge preservation graft will be covered with a non-resorbable PTFE membrane during the surgery.

PROCEDURE

Acellular dermal matrix

The ridge preservation graft will be covered with an acellular dermal matrix allograft during the surgery.

Sponsors & Collaborators

  • University of Louisville

    lead OTHER

Principal Investigators

  • Henry Greenwell, DMD · University of Louisville

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2014-07-31
Completion
2014-07-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01905280 on ClinicalTrials.gov