Furcation Defects Clinical Trial
Official title:
Piezosurgery in the Treatment of Class II Furcation Involvement
| Verified date | February 2017 |
| Source | University of Trieste |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
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
| Status | Active, not recruiting |
| Enrollment | 30 |
| Est. completion date | November 2017 |
| Est. primary completion date | October 2015 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
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 |
| Country | Name | City | State |
|---|---|---|---|
| Italy | Matteo Visintin | Trieste | TS |
| Lead Sponsor | Collaborator |
|---|---|
| Matteo Visintin |
Italy,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Horizontal probing depth (PH) | horizontal probing depth | 180 days | |
| Secondary | Plaque index (PI) | plaque index | 180 days | |
| Secondary | Bleeding on probing (BoP) | bleeding on probing | 180 days | |
| Secondary | Pocket probing depth (PPD) | pocket probing depth | 180 days | |
| Secondary | Furcation closure (FC) | furcation closure | 180 days | |
| Secondary | Clinical attachment level (CAL) | clinical attachment level | 180 days |
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