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

H

Hams Hamed Abdelrahman

Status

Completed

Conditions

Furcation Defects

Treatments

Other: Hydroxyapatite bone graft
Other: PD VitalOs cement®
Other: biodegardable collagen membrane

Study type

Interventional

Funder types

Other

Identifiers

NCT04443972
Furcation invlvement

Details and patient eligibility

About

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.

Full 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.

Enrollment

14 patients

Sex

All

Ages

30 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • • Presence of a lower molar with critical size grade II furcation defect (15) with a horizontal component of 4 mm and a vertical component of 4 to 6 mm (18), detected using Naber's probe and William's periodontal probe.

    • Patient's age between 30 - 50 years.
    • Both sexes.
    • The patient should be psychologically accepting the procedures.
    • Patients should be systemically free.

Exclusion criteria

  • • Uncooperative patients regarding oral hygiene measures performance.

    • Patients with para functional habits.
    • Smokers.
    • Pregnant or lactating women.
    • Patients who underwent any periodontal surgeries in the study site during the six months prior to study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

14 participants in 2 patient groups

PD VitalOs cement® alone
Experimental group
Description:
class II furcation defects that will be treated with PD VitalOs cement® alone
Treatment:
Other: PD VitalOs cement®
PD VitalOs cement® plus Bone graft and membrane
Experimental group
Description:
PD VitalOs cement® and Hydroxyapatite bone graft and biodegradable collagen membrane in the treatment of class II furcation defects.
Treatment:
Other: PD VitalOs cement®
Other: Hydroxyapatite bone graft
Other: biodegardable collagen membrane

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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