Clinical Trials Directory

Trials / Completed

CompletedNCT04443972

Evaluation of Injectable Beta-tricalcium Phosphate Clinically in Treatment of Grade II Furcation Involvement

Evaluation of Injectable Beta- Tricalcium Phosphate as an Occlusive Barrier Membrane in Treatment of Grade ii Furcation Involvement (Clinical and Radiographic Study)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
14 (actual)
Sponsor
Hams Hamed Abdelrahman · Academic / Other
Sex
All
Age
30 Years – 50 Years
Healthy volunteers
Accepted

Summary

This study will be conducted to evaluate clinically and radiographically the use of PD VitalOs cement® bone graft in the treatment of class II furcation defects comparing with Hydroxyapatite bone graft and biodegradable collagen membrane in the treatment of class II furcation defects.

Detailed description

The study is a randomized, controlled clinical trial. Patients were randomly divided into two equal groups, Group I (Test group): included seven Grade II furcation defects treated by beta tricalcium phosphate bone cement only. Group II (Control group): included seven Grade II furcation defects treated with granulated beta tricalcium phosphate bone graft covered by resorbable collagen membrane.

Conditions

Interventions

TypeNameDescription
OTHERPD VitalOs cement®PD VitalOs cement®\* is a synthetic bone grafting cement designed for bone void filling and bone regeneration in dental surgery
OTHERHydroxyapatite bone grafta bioceramic bone substitute, providing a scaffold for bone deposition
OTHERbiodegardable collagen membraneprovide efficacious barriers that were interposed between the flap and root surface.

Timeline

Start date
2018-04-12
Primary completion
2019-07-10
Completion
2020-02-04
First posted
2020-06-23
Last updated
2020-06-23

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04443972. Inclusion in this directory is not an endorsement.