RPCEC00000212CompletedPhase 4
Effectiveness and safety of Biograft-G in bone repair of the bucal complex. - EB-1
Biomaterials Center, University of Havana0 sitesStarted: March 11, 2016Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- N/a: Single Arm Study. Masking: Open. Control Group: Uncontrolled. Assignment: Single Group. Purpose: Treatment
Eligibility Criteria
- Ages
- 18 years to 75 years (—)
- Sex
- All
Inclusion Criteria
- •1- Patients who meet the established diagnostic criteria.
- •2- Age range between 18 and 75 years, both sexes, Cuban citizen without distinction of race.
- •3- Outpatient whose health allows them to perform a normal physical activity without restrictions or light work.
- •4- Patients that can be treated surgically.
- •5- Patients give their written consent for participation to be included
- •6- Patients with periodontal infra bony origin involved bone defects whose teeth have no mobility than Grade 2 according to Miller’s classification
Exclusion Criteria
- •1- Diabetic patients decompensated or difficult to control.
- •2- Immunocompromised or patients under immunosuppressive therapy.
- •3- Mentally retarded.
- •4- Patients with malignancies diagnosed, from any location.
- •5- Patients who are pregnant.
- •6- Patients with conditions of smoking and alcoholism.
- •7- Patients with difficulties in tracking for residing in distant places.
- •8- Patients who refuse to be included in the investigation.
- •9- Patients with horizontal bone loss or periodontal defects supraóseos origin
Investigators
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