Clinical Trials Directory

Trials / Completed

CompletedNCT03354182

Surgical Treatment of Mandibular Furcations Using a Xenograft With/Without a Collagen Membrane

Treatment of Mandibular Type II Furcations Using Bovine-derived Bone Xenograft With or Without a Collagen Membrane: a Randomized Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
19 (actual)
Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of the study was to perform a randomized controlled clinical study in order to compare the effects of a bovine derived xenograft (with 10% collagen) + a bioabsorbable membrane (control group, CG) vs a bovine derived xenograft (with 10% collagen) alone (test group, TG) on the surgical treatment of mandibular type II furcation defects.

Detailed description

The aim of the study was to perform a randomized controlled clinical study in order to compare the effects of a bovine derived xenograft (with 10% collagen) + a bioabsorbable membrane (control group, CG) vs a bovine derived xenograft (with 10% collagen) alone (test group, TG) on the surgical treatment of mandibular type II furcation defects. The patients all underwent the same surgical intervention with the only difference between the two groups being the use or not of a collagen membrane.

Conditions

Interventions

TypeNameDescription
PROCEDUREOpen flap surgeryElevation of a flap in order to access the treated furcation
DEVICEBio-oss collagenBiomaterial for periodontal surgery
DEVICEBio-gideBiomaterial for periodontal surgery

Timeline

Start date
2015-07-30
Primary completion
2017-01-02
Completion
2017-01-02
First posted
2017-11-27
Last updated
2017-12-02

Source: ClinicalTrials.gov record NCT03354182. Inclusion in this directory is not an endorsement.