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Comparing the Efficacy and Morbidity of Two Vertical Ridge Augmentation Techniques

NCT02703480 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2024-09-04

Study results available
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Summary

The proposed study design is a randomized controlled trial, split mouth design, to compare the two different vertical augmentation procedures: Titanium mesh (Ti-mesh) technique and Guided Bone Regeneration (GBR) technique with a high-density polytetrafluoroethylene (d-PTFE) membrane.

Conditions

  • Vertical Alveolar Bone Loss

Interventions

BIOLOGICAL

d-PTFE

high-density polytetrafluoroethylene (d-PTFE) membrane

BIOLOGICAL

Ti-mesh

Titanium mesh

Sponsors & Collaborators

  • Tufts University

    lead OTHER

Principal Investigators

  • Yumi Ogata, DMD, DDS, MS · Tufts University School of Dental Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-12-31
Primary Completion
2018-03-31
Completion
2025-06-30

Countries

  • United States

Study Locations

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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 NCT02703480 on ClinicalTrials.gov