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

NCT03354182 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 19

Last updated 2017-12-02

No results posted yet for this study

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.

Conditions

  • Furcation Defects

Interventions

PROCEDURE

Open flap surgery

Elevation of a flap in order to access the treated furcation

DEVICE

Bio-oss collagen

Biomaterial for periodontal surgery

DEVICE

Bio-gide

Biomaterial for periodontal surgery

Sponsors & Collaborators

  • Cliniques universitaires Saint-Luc- Université Catholique de Louvain

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-07-30
Primary Completion
2017-01-02
Completion
2017-01-02

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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 NCT03354182 on ClinicalTrials.gov