Piezosurgery in the Treatment of Class II Furcation Involvement

NCT ID: NCT02132806

Last Updated: 2017-02-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-03-31

Study Completion Date

2017-11-30

Brief Summary

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The purpose of this study is to evaluate the effectiveness of piezosurgery in the treatment of class II furcation involvement using biomaterials and new surgical techniques

Detailed Description

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Conditions

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Furcation Defects

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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OFD with piezosurgery

Open flap debridement with Piezosurgery

Group Type EXPERIMENTAL

Piezosurgery

Intervention Type PROCEDURE

OFD with piezosurgery+biomaterial

Open flap debridement with Piezosurgery with biomaterial mp3

Group Type EXPERIMENTAL

Piezosurgery with biomaterial mp3

Intervention Type PROCEDURE

OFD with piezosurgery+mp3+bracket

Open flap debridement with Piezosurgery with biomaterial mp3 + bracket

Group Type EXPERIMENTAL

Piezosurgery with biomaterial mp3 + bracket

Intervention Type PROCEDURE

Interventions

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Piezosurgery with biomaterial mp3 + bracket

Intervention Type PROCEDURE

Piezosurgery with biomaterial mp3

Intervention Type PROCEDURE

Piezosurgery

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* previous subgingival instrumentation with adequate plaque control (FMPS \< 20%) and bleeding on probing (FMBS \< 20%).
* one or more mandibular molar with buccal class-II furcation involvement

Exclusion Criteria

* diabetes mellitus
* pregnancy and lactation period
* subjects smoking \> 10 cigarettes/day were excluded
* subjects in chronically treatment with calcium antagonist, immunosuppressive drugs and Antiepileptic Drugs
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Matteo Visintin

OTHER

Sponsor Role lead

Responsible Party

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Matteo Visintin

Student

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Matteo Visintin

Role: PRINCIPAL_INVESTIGATOR

UCO Clinica Odontoiatrica e Stomatologica - Ospedale Maggiore Trieste

Locations

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Matteo Visintin

Trieste, TS, Italy

Site Status

Countries

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Italy

Other Identifiers

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UNITS01-2014

Identifier Type: -

Identifier Source: org_study_id

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