At a glance
ClinicalIndex Comparison RecordN/AActive· 11 enrolled
Drug / intervention
d-PTFE +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Comparison of d-PTFE Membrane With Titanium-mesh in Vertical Ridge Augmentation: A Split Mouth, Randomized Controlled Clinical Trial
In Brief
A clinical study evaluating d-PTFE and Ti-mesh for Vertical Alveolar Bone Loss. Active but no longer recruiting, targeting 11 participants across 1 site.
Detailed 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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsVertical Alveolar Bone Loss
CountriesUnited States
Collaborators--
Timeline
N/AActiveOverdue
20162017201820192020202120222023202420252026
Enrollment StartDec 2015
First PostedMar 2016
Primary CompletionMar 2018
Study CompletionJun 2025
TodayJul 2026
First PostedMar 9, 2016
Enrollment StartDec 1, 2015
Primary CompletionMar 1, 2018
Study CompletionJun 1, 2025
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 10.3 years ago
Interventions
d-PTFEbiological
high-density polytetrafluoroethylene (d-PTFE) membrane
Ti-meshbiological
Titanium mesh